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The dataset generation failed
Error code: DatasetGenerationError
Exception: CastError
Message: Couldn't cast
product_description: string
reason_for_recall: string
recall_initiation: string
status: string
classification: string
voluntary_mandated: string
source: string
submissions: null
products: null
openfda: string
sponsor_name: string
application_number: string
to
{'submissions': List(Json(decode=True)), 'application_number': Value('string'), 'sponsor_name': Value('string'), 'products': List(Json(decode=True)), 'source': Value('string'), 'openfda': Json(decode=True)}
because column names don't match
Traceback: Traceback (most recent call last):
File "/usr/local/lib/python3.12/site-packages/datasets/builder.py", line 1779, in _prepare_split_single
for key, table in generator:
^^^^^^^^^
File "/src/services/worker/src/worker/job_runners/config/parquet_and_info.py", line 609, in wrapped
for item in generator(*args, **kwargs):
^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.12/site-packages/datasets/packaged_modules/json/json.py", line 299, in _generate_tables
self._cast_table(pa_table, json_field_paths=json_field_paths),
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.12/site-packages/datasets/packaged_modules/json/json.py", line 128, in _cast_table
pa_table = table_cast(pa_table, self.info.features.arrow_schema)
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.12/site-packages/datasets/table.py", line 2321, in table_cast
return cast_table_to_schema(table, schema)
^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.12/site-packages/datasets/table.py", line 2249, in cast_table_to_schema
raise CastError(
datasets.table.CastError: Couldn't cast
product_description: string
reason_for_recall: string
recall_initiation: string
status: string
classification: string
voluntary_mandated: string
source: string
submissions: null
products: null
openfda: string
sponsor_name: string
application_number: string
to
{'submissions': List(Json(decode=True)), 'application_number': Value('string'), 'sponsor_name': Value('string'), 'products': List(Json(decode=True)), 'source': Value('string'), 'openfda': Json(decode=True)}
because column names don't match
The above exception was the direct cause of the following exception:
Traceback (most recent call last):
File "/src/services/worker/src/worker/job_runners/config/parquet_and_info.py", line 1342, in compute_config_parquet_and_info_response
parquet_operations, partial, estimated_dataset_info = stream_convert_to_parquet(
^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/src/services/worker/src/worker/job_runners/config/parquet_and_info.py", line 907, in stream_convert_to_parquet
builder._prepare_split(split_generator=splits_generators[split], file_format="parquet")
File "/usr/local/lib/python3.12/site-packages/datasets/builder.py", line 1646, in _prepare_split
for job_id, done, content in self._prepare_split_single(
^^^^^^^^^^^^^^^^^^^^^^^^^^^
File "/usr/local/lib/python3.12/site-packages/datasets/builder.py", line 1832, in _prepare_split_single
raise DatasetGenerationError("An error occurred while generating the dataset") from e
datasets.exceptions.DatasetGenerationError: An error occurred while generating the datasetNeed help to make the dataset viewer work? Make sure to review how to configure the dataset viewer, and open a discussion for direct support.
submissions list | application_number string | sponsor_name string | products list | source string | openfda unknown |
|---|---|---|---|---|---|
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20050831"
}
] | ANDA076191 | BARR | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "FEXOFENADINE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "FEXOFENADINE HYDROCHLORIDE",
"strength": "60MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20020207"
}
] | ANDA076193 | NESHER PHARMS | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "PROPAFENONE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "PROPAFENONE HYDROCHLORIDE",
"strength": "150MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "7",
"submission_status": "AP",
"submission_status_date": "20080918",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"submission_number": "3",
"submission... | ANDA076207 | FRESENIUS KABI USA | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "PAMIDRONATE DISODIUM",
"active_ingredients": [
{
"name": "PAMIDRONATE DISODIUM",
"strength": "90MG/10ML (9MG/ML)"
}
],
"reference_standard": "No",
"dosage_form": "INJECTABLE",
"route": "INJE... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "12",
"submission_status": "AP",
"submission_status_date": "20071015",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submission_number": "1",
"submission... | ANDA076217 | MYLAN INSTITUTIONAL | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "AMIODARONE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "AMIODARONE HYDROCHLORIDE",
"strength": "50MG/ML"
}
],
"reference_standard": "Yes",
"dosage_form": "INJECTABLE",
"route": "INJECT... | drug_drugsfda | {
"application_number": [
"ANDA076217"
],
"brand_name": [
"AMIODARONE HYDROCHLORIDE"
],
"generic_name": [
"AMIODARONE HYDROCHLORIDE"
],
"manufacturer_name": [
"Mylan Institutional LLC"
],
"product_ndc": [
"72078-046",
"67457-153"
],
"product_type": [
"HUMAN PRESCRIPTION... |
[
{
"submission_type": "SUPPL",
"submission_number": "8",
"submission_status": "AP",
"submission_status_date": "20150107",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"submi... | ANDA076221 | BARR LABS INC | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL",
"active_ingredients": [
{
"name": "ETHINYL ESTRADIOL",
"strength": "0.005MG"
},
{
"name": "NORETHINDRONE ACETATE",
"strength": "1MG"
... | drug_drugsfda | {
"application_number": [
"ANDA076221"
],
"brand_name": [
"JINTELI"
],
"generic_name": [
"NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL"
],
"manufacturer_name": [
"Teva Pharmaceuticals USA, Inc."
],
"product_ndc": [
"0093-3122"
],
"product_type": [
"HUMAN PRESCRIPTION DRUG"
... |
[
{
"submission_type": "SUPPL",
"submission_number": "6",
"submission_status": "AP",
"submission_status_date": "20210505",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submis... | ANDA076222 | HIKMA | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "GANCICLOVIR SODIUM",
"active_ingredients": [
{
"name": "GANCICLOVIR SODIUM",
"strength": "EQ 500MG BASE/VIAL"
}
],
"reference_standard": "No",
"dosage_form": "INJECTABLE",
"route": "INJECTIO... | drug_drugsfda | {
"application_number": [
"ANDA076222"
],
"brand_name": [
"GANCICLOVIR"
],
"generic_name": [
"GANCICLOVIR SODIUM"
],
"manufacturer_name": [
"Hikma Pharmaceuticals USA Inc."
],
"product_ndc": [
"0143-9299"
],
"product_type": [
"HUMAN PRESCRIPTION DRUG"
],
"route": [
... |
[
{
"submission_type": "SUPPL",
"submission_number": "14",
"submission_status": "AP",
"submission_status_date": "20251010",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submi... | ANDA076225 | DR REDDYS LABS SA | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "ERRIN",
"active_ingredients": [
{
"name": "NORETHINDRONE",
"strength": "0.35MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL-28",
"marketing_status": "Prescri... | drug_drugsfda | {
"application_number": [
"ANDA076225"
],
"brand_name": [
"ERRIN"
],
"generic_name": [
"NORETHINDRONE"
],
"manufacturer_name": [
"Mayne Pharma Inc.",
"Dr. Reddy's Labratories Inc."
],
"product_ndc": [
"51862-886",
"75907-075"
],
"product_type": [
"HUMAN PRESCRIPTION... |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20030828"
}
] | ANDA076234 | IMPAX PHARMS | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "FLAVOXATE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "FLAVOXATE HYDROCHLORIDE",
"strength": "100MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"mar... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20040730"
}
] | ANDA076249 | IMPAX LABS | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "METFORMIN HYDROCHLORIDE",
"active_ingredients": [
{
"name": "METFORMIN HYDROCHLORIDE",
"strength": "500MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET, EXTENDED RELEASE",
"route"... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20050518",
"application_docs": [
{
"id": "23811",
"url": "http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm109352.htm",
... | ANDA076251 | BARR | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "FLUOXETINE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "FLUOXETINE HYDROCHLORIDE",
"strength": "EQ 40MG BASE"
}
],
"reference_standard": "No",
"dosage_form": "CAPSULE",
"route": "ORAL"... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "32",
"submission_status": "AP",
"submission_status_date": "20231020",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076262 | AIPING PHARM INC | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "LISINOPRIL AND HYDROCHLOROTHIAZIDE",
"active_ingredients": [
{
"name": "HYDROCHLOROTHIAZIDE",
"strength": "12.5MG"
},
{
"name": "LISINOPRIL",
"strength": "20MG"
}
],
"ref... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20041006"
},
{
"submission_type": "SUPPL",
"submission_number": "7",
"submission_status": "AP",
"submission_status_date": "20191028",
"review_priority": "STANDARD",
... | ANDA076271 | SANDOZ | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "KETOROLAC TROMETHAMINE",
"active_ingredients": [
{
"name": "KETOROLAC TROMETHAMINE",
"strength": "15MG/ML"
}
],
"reference_standard": "No",
"dosage_form": "INJECTABLE",
"route": "INJECTION",... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20030114"
},
{
"submission_type": "SUPPL",
"submission_number": "5",
"submission_status": "AP",
"submission_status_date": "20150217",
"submission_class_code": "MANUF (... | ANDA076278 | HIKMA | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "FLECAINIDE ACETATE",
"active_ingredients": [
{
"name": "FLECAINIDE ACETATE",
"strength": "50MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_stat... | drug_drugsfda | {
"application_number": [
"ANDA076278"
],
"brand_name": [
"FLECAINIDE ACETATE"
],
"generic_name": [
"FLECAINIDE ACETATE"
],
"manufacturer_name": [
"Hikma Pharmaceuticals USA Inc."
],
"product_ndc": [
"0054-0010",
"0054-0011",
"0054-0012"
],
"product_type": [
"HUMAN ... |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20021220"
}
] | ANDA076296 | FRESENIUS KABI USA | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "VINCRISTINE SULFATE",
"active_ingredients": [
{
"name": "VINCRISTINE SULFATE",
"strength": "1MG/ML"
}
],
"reference_standard": "No",
"dosage_form": "INJECTABLE",
"route": "INJECTION",
"m... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "25",
"submission_status": "AP",
"submission_status_date": "20110923",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submission_number": "1",
"submission... | ANDA076301 | PERRIGO | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "LORATADINE",
"active_ingredients": [
{
"name": "LORATADINE",
"strength": "10MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_status": "Over-the-c... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "2",
"submission_status": "AP",
"submission_status_date": "20100128",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"submission_number": "9",
"submission... | ANDA076317 | TEVA | [
{
"product_number": "004",
"reference_drug": "No",
"brand_name": "TOPIRAMATE",
"active_ingredients": [
{
"name": "TOPIRAMATE",
"strength": "200MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_status": "Discontin... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20040930"
}
] | ANDA076321 | ANI PHARMS | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "TIZANIDINE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "TIZANIDINE HYDROCHLORIDE",
"strength": "EQ 4MG BASE"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
... | drug_drugsfda | null |
null | NDA017408 | GD SEARLE LLC | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "CU-7",
"active_ingredients": [
{
"name": "COPPER",
"strength": "89MG"
}
],
"reference_standard": "No",
"dosage_form": "INTRAUTERINE DEVICE",
"route": "INTRAUTERINE",
"marketing_status": ... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "19740918",
"review_priority": "STANDARD",
"submission_class_code": "TYPE 3",
"submission_class_code_description": "Type 3 - New Dosage Form"
}
] | NDA017411 | HUNTINGTON LABS | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "HEXA-GERM",
"active_ingredients": [
{
"name": "HEXACHLOROPHENE",
"strength": "3%"
}
],
"reference_standard": "No",
"dosage_form": "EMULSION",
"route": "TOPICAL",
"marketing_status": "Dis... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "11",
"submission_status": "AP",
"submission_status_date": "20090327",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submission_number": "1",
"submission... | ANDA076348 | ANI PHARMS | [
{
"product_number": "003",
"reference_drug": "No",
"brand_name": "BENAZEPRIL HYDROCHLORIDE AND HYDROCHLOROTHIAZIDE",
"active_ingredients": [
{
"name": "BENAZEPRIL HYDROCHLORIDE",
"strength": "20MG"
},
{
"name": "HYDROCHLOROTHIAZIDE",
"strength": "12.... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "30",
"submission_status": "AP",
"submission_status_date": "20170821",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076357 | PERRIGO | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "MICONAZOLE 3 COMBINATION PACK",
"active_ingredients": [
{
"name": "MICONAZOLE NITRATE",
"strength": "2%,4%"
}
],
"reference_standard": "No",
"dosage_form": "CREAM",
"route": "TOPICAL, VAGINA... | drug_drugsfda | {
"application_number": [
"ANDA076357"
],
"brand_name": [
"MICONAZOLE 3",
"LEADER MICONAZOLE 3",
"UP AND UP MICONAZOLE 3",
"FOSTER AND THRIVE MICONAZOLE 3",
"RUGBY MICONAZOLE 3"
],
"generic_name": [
"MICONAZOLE NITRATE"
],
"manufacturer_name": [
"Rite Aid Corporation",
... |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "19770222",
"review_priority": "STANDARD",
"submission_class_code": "TYPE 5",
"submission_class_code_description": "Type 5 - New Formulation or New Manufacturer"
},
{
"subm... | NDA017413 | 3M | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "SCRUBTEAM SURGICAL SPONGEBRUSH",
"active_ingredients": [
{
"name": "HEXACHLOROPHENE",
"strength": "330MG"
}
],
"reference_standard": "No",
"dosage_form": "SPONGE",
"route": "TOPICAL",
"m... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "26",
"submission_status": "AP",
"submission_status_date": "20230925",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076381 | BARR | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "JUNEL 1.5/30",
"active_ingredients": [
{
"name": "ETHINYL ESTRADIOL",
"strength": "0.03MG"
},
{
"name": "NORETHINDRONE ACETATE",
"strength": "1.5MG"
}
],
"reference_stand... | drug_drugsfda | {
"application_number": [
"ANDA076381"
],
"brand_name": [
"JUNEL 21 DAY",
"LOESTRIN 21 DAY"
],
"generic_name": [
"NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL"
],
"manufacturer_name": [
"Teva Pharmaceuticals USA, Inc.",
"Teva Women's Health LLC"
],
"product_ndc": [
"0555-902... |
[
{
"submission_type": "SUPPL",
"submission_number": "28",
"submission_status": "AP",
"submission_status_date": "20160930",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076388 | TEVA | [
{
"product_number": "004",
"reference_drug": "No",
"brand_name": "LAMOTRIGINE",
"active_ingredients": [
{
"name": "LAMOTRIGINE",
"strength": "200MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_status": "Discont... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20050418",
"application_docs": [
{
"id": "8909",
"url": "http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/076417ltr.pdf",
"date": "20050428",
... | ANDA076417 | WATSON LABS | [
{
"product_number": "002",
"reference_drug": "No",
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... | drug_drugsfda | null |
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"submission_status_date": "20130227",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submis... | ANDA076675 | PH HEALTH | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "EMOQUETTE",
"active_ingredients": [
{
"name": "DESOGESTREL",
"strength": "0.15MG"
},
{
"name": "ETHINYL ESTRADIOL",
"strength": "0.03MG"
}
],
"reference_standard": "No",
... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20050418",
"application_docs": [
{
"id": "31154",
"url": "http://www.accessdata.fda.gov/drugsatfda_docs/appletter/2005/076683ltr.pdf",
"date": "20050428",
... | ANDA076683 | CHARTWELL RX | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "ANAGRELIDE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "ANAGRELIDE HYDROCHLORIDE",
"strength": "EQ 0.5MG BASE"
}
],
"reference_standard": "No",
"dosage_form": "CAPSULE",
"route": "ORAL... | drug_drugsfda | {
"application_number": [
"ANDA076683"
],
"brand_name": [
"ANAGRELIDE"
],
"generic_name": [
"ANAGRELIDE"
],
"manufacturer_name": [
"Chartwell RX, LLC"
],
"product_ndc": [
"62135-312",
"62135-313"
],
"product_type": [
"HUMAN PRESCRIPTION DRUG"
],
"route": [
"ORAL... |
null | NDA017460 | CALGON | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "SEPTI-SOFT",
"active_ingredients": [
{
"name": "HEXACHLOROPHENE",
"strength": "0.25%"
}
],
"reference_standard": "No",
"dosage_form": "SOLUTION",
"route": "TOPICAL",
"marketing_status": ... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "13",
"submission_status": "AP",
"submission_status_date": "20251023",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076694 | PHARMOBEDIENT | [
{
"product_number": "004",
"reference_drug": "No",
"brand_name": "QUINAPRIL HYDROCHLORIDE",
"active_ingredients": [
{
"name": "QUINAPRIL HYDROCHLORIDE",
"strength": "EQ 40MG BASE"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "41",
"submission_status": "AP",
"submission_status_date": "20240603",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076704 | MYLAN | [
{
"product_number": "004",
"reference_drug": "No",
"brand_name": "METOPROLOL TARTRATE",
"active_ingredients": [
{
"name": "METOPROLOL TARTRATE",
"strength": "37.5MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_... | drug_drugsfda | {
"application_number": [
"ANDA076704"
],
"brand_name": [
"METOPROLOL TARTRATE"
],
"generic_name": [
"METOPROLOL TARTRATE"
],
"manufacturer_name": [
"Mylan Pharmaceuticals Inc."
],
"product_ndc": [
"0378-0018",
"0378-4593",
"0378-0032",
"0378-4594",
"0378-0047"
],... |
[
{
"submission_type": "SUPPL",
"submission_number": "8",
"submission_status": "AP",
"submission_status_date": "20160926",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"submi... | ANDA076708 | DR REDDYS LABS LTD | [
{
"product_number": "004",
"reference_drug": "No",
"brand_name": "LAMOTRIGINE",
"active_ingredients": [
{
"name": "LAMOTRIGINE",
"strength": "200MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_status": "Prescri... | drug_drugsfda | {
"application_number": [
"ANDA076708"
],
"brand_name": [
"LAMOTRIGINE"
],
"generic_name": [
"LAMOTRIGINE"
],
"manufacturer_name": [
"Dr.Reddy's Laboratories Limited"
],
"product_ndc": [
"55111-220",
"55111-221",
"55111-222",
"55111-223"
],
"product_type": [
"HU... |
[
{
"submission_type": "SUPPL",
"submission_number": "9",
"submission_status": "AP",
"submission_status_date": "19800716",
"review_priority": "STANDARD",
"submission_class_code": "MANUF (CMC)",
"submission_class_code_description": "Manufacturing (CMC)"
},
{
"submission_type": "SUPP... | NDA017464 | B BRAUN | [
{
"product_number": "001",
"reference_drug": "Yes",
"brand_name": "SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER",
"active_ingredients": [
{
"name": "SODIUM CHLORIDE",
"strength": "900MG/100ML"
}
],
"reference_standard": "Yes",
"dosage_form": "INJECTABLE",
"ro... | drug_drugsfda | {
"application_number": [
"NDA017464"
],
"brand_name": [
"SODIUM CHLORIDE"
],
"generic_name": [
"SODIUM CHLORIDE"
],
"manufacturer_name": [
"B. Braun Medical Inc."
],
"product_ndc": [
"0264-1800"
],
"product_type": [
"HUMAN PRESCRIPTION DRUG"
],
"route": [
"INTRAVEN... |
[
{
"submission_type": "SUPPL",
"submission_number": "12",
"submission_status": "AP",
"submission_status_date": "20241031",
"submission_class_code": "REMS",
"submission_class_code_description": "REMS"
},
{
"submission_type": "SUPPL",
"submission_number": "10",
"submission_statu... | ANDA076723 | MPP PHARMA | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "HYDROMORPHONE HYDROCHLORIDE",
"active_ingredients": [
{
"name": "HYDROMORPHONE HYDROCHLORIDE",
"strength": "8MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "4",
"submission_status": "AP",
"submission_status_date": "20091106",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_... | ANDA076739 | SUN PHARM INDS LTD | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "FOSINOPRIL SODIUM AND HYDROCHLOROTHIAZIDE",
"active_ingredients": [
{
"name": "FOSINOPRIL SODIUM",
"strength": "10MG"
},
{
"name": "HYDROCHLOROTHIAZIDE",
"strength": "12.5MG"
}
... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "29",
"submission_status": "AP",
"submission_status_date": "20021204",
"review_priority": "STANDARD",
"submission_class_code": "MANUF (CMC)",
"submission_class_code_description": "Manufacturing (CMC)"
},
{
"submission_type": "SUP... | NDA017469 | SANDOZ | [
{
"product_number": "001",
"reference_drug": "Yes",
"brand_name": "OMNIPRED",
"active_ingredients": [
{
"name": "PREDNISOLONE ACETATE",
"strength": "1%"
}
],
"reference_standard": "Yes",
"dosage_form": "SUSPENSION/DROPS",
"route": "OPHTHALMIC",
"market... | drug_drugsfda | {
"application_number": [
"NDA017469"
],
"brand_name": [
"PREDNISOLONE ACETATE"
],
"generic_name": [
"PREDNISOLONE ACETATE"
],
"manufacturer_name": [
"Sandoz Inc"
],
"product_ndc": [
"61314-637"
],
"product_type": [
"HUMAN PRESCRIPTION DRUG"
],
"route": [
"OPHTHALMI... |
[
{
"submission_type": "SUPPL",
"submission_number": "16",
"submission_status": "AP",
"submission_status_date": "20240216",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076766 | BAXTER HLTHCARE | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "FLUCONAZOLE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER",
"active_ingredients": [
{
"name": "FLUCONAZOLE",
"strength": "400MG/200ML (2MG/ML)"
}
],
"reference_standard": "No",
"dosage_form": "IN... | drug_drugsfda | {
"application_number": [
"ANDA076766"
],
"brand_name": [
"FLUCONAZOLE"
],
"generic_name": [
"FLUCONAZOLE"
],
"manufacturer_name": [
"Baxter Healthcare Company"
],
"product_ndc": [
"0338-6045",
"0338-6046"
],
"product_type": [
"HUMAN PRESCRIPTION DRUG"
],
"route": [... |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20100628"
}
] | ANDA076797 | PRECISION DOSE | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "RISPERIDONE",
"active_ingredients": [
{
"name": "RISPERIDONE",
"strength": "1MG/ML"
}
],
"reference_standard": "No",
"dosage_form": "SOLUTION",
"route": "ORAL",
"marketing_status": "Disc... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20040825"
}
] | ANDA076814 | ABLE | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "DEXTROAMPHETAMINE SULFATE",
"active_ingredients": [
{
"name": "DEXTROAMPHETAMINE SULFATE",
"strength": "10MG"
}
],
"reference_standard": "No",
"dosage_form": "CAPSULE, EXTENDED RELEASE",
"ro... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20040831"
},
{
"submission_type": "SUPPL",
"submission_number": "8",
"submission_status": "AP",
"submission_status_date": "20200715",
"review_priority": "STANDARD",
... | ANDA076830 | ALVOGEN | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "OFLOXACIN",
"active_ingredients": [
{
"name": "OFLOXACIN",
"strength": "0.3%"
}
],
"reference_standard": "No",
"dosage_form": "SOLUTION/DROPS",
"route": "OPHTHALMIC",
"marketing_status":... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "17",
"submission_status": "AP",
"submission_status_date": "20251106",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | ANDA076834 | CHARTWELL RX | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "BUPROPION HYDROCHLORIDE",
"active_ingredients": [
{
"name": "BUPROPION HYDROCHLORIDE",
"strength": "150MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET, EXTENDED RELEASE",
"route"... | drug_drugsfda | null |
[
{
"submission_type": "SUPPL",
"submission_number": "13",
"submission_status": "AP",
"submission_status_date": "20130502",
"review_priority": "UNKNOWN",
"submission_class_code": "MANUF (CMC)",
"submission_class_code_description": "Manufacturing (CMC)"
},
{
"submission_type": "SUPP... | ANDA076846 | TEVA | [
{
"product_number": "003",
"reference_drug": "No",
"brand_name": "AMLODIPINE BESYLATE",
"active_ingredients": [
{
"name": "AMLODIPINE BESYLATE",
"strength": "EQ 10MG BASE"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"mark... | drug_drugsfda | {
"application_number": [
"ANDA076846"
],
"brand_name": [
"AMLODIPINE BESYLATE"
],
"generic_name": [
"AMLODIPINE BESYLATE"
],
"manufacturer_name": [
"Teva Pharmaceuticals, Inc."
],
"product_ndc": [
"0480-0083",
"0480-7167",
"0480-7168"
],
"product_type": [
"HUMAN PR... |
[
{
"submission_type": "SUPPL",
"submission_number": "84",
"submission_status": "AP",
"submission_status_date": "19990827",
"review_priority": "STANDARD",
"submission_class_code": "LABELING",
"submission_class_code_description": "Labeling"
},
{
"submission_type": "SUPPL",
"subm... | NDA017489 | ORTHO MCNEIL PHARM | [
{
"product_number": "002",
"reference_drug": "No",
"brand_name": "ORTHO-NOVUM 1/35-21",
"active_ingredients": [
{
"name": "ETHINYL ESTRADIOL",
"strength": "0.035MG"
},
{
"name": "NORETHINDRONE",
"strength": "1MG **Federal Register determination that ... | drug_drugsfda | null |
[
{
"submission_type": "ORIG",
"submission_number": "1",
"submission_status": "AP",
"submission_status_date": "20040721"
}
] | ANDA076891 | WATSON LABS | [
{
"product_number": "001",
"reference_drug": "No",
"brand_name": "METOLAZONE",
"active_ingredients": [
{
"name": "METOLAZONE",
"strength": "10MG"
}
],
"reference_standard": "No",
"dosage_form": "TABLET",
"route": "ORAL",
"marketing_status": "Discontinu... | drug_drugsfda | null |
End of preview.
OpenFDA Drug Interaction & Safety Dataset
TechFryz · Emmanuel Bain Oduwo · Kemirix v1.0
Complete OpenFDA dataset processed for the Kemirix Clinical Decision Support System.
Stream-processed from 1,483 raw ZIP files (59GB) into clean JSONL (8-12GB).
Dataset Contents
| File | Description | Records |
|---|---|---|
drug_events_2012_2026.jsonl |
FAERS adverse event reports 2012–2026 | Millions |
drug_labels.jsonl |
257,727 FDA prescribing labels | 257K+ |
drug_enforcement.jsonl |
Drug recalls (Class I/II/III) | Thousands |
drug_shortages.jsonl |
Active drug shortage alerts | Thousands |
drug_ndc.jsonl |
NDC drug code cross-reference | Thousands |
drug_drugsfda.jsonl |
FDA approval data | Thousands |
food_events.jsonl |
Food adverse events | Thousands |
food_enforcement.jsonl |
Food recalls | Thousands |
Usage
from datasets import load_dataset
ds = load_dataset("Oduwo/Open-FDA-Approved-drug-interactions", data_files="drug_labels.jsonl")
Built for Africa. Bi'idhnillahi Ta'ala.
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