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United States · US · US:71335-0581_71bf33e7-049d-4d2d-a83c-ed205142f17d
Clopidogrel
Orange BookUNIISPLATC B01AC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBryant Ranch Prepack
CountryUS (United States)
ATC codeB01AC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11713350581190 TABLET in 1 BOTTLE (71335-0581-1)
- ndc11713350581230 TABLET in 1 BOTTLE (71335-0581-2)
- ndc11713350581360 TABLET in 1 BOTTLE (71335-0581-3)
- ndc11713350581420 TABLET in 1 BOTTLE (71335-0581-4)
- ndc11713350581510 TABLET in 1 BOTTLE (71335-0581-5)
Annotations
UNII (FDA Substance ID)
08I79HTP27
CLOPIDOGREL BISULFATE
RxCUI 236991
Orange Book
A202928
AB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "08I79HTP27",
"rxcui": "236991",
"inchikey": "FDEODCTUSIWGLK-RSAXXLAASA-N",
"display_name": "CLOPIDOGREL BISULFATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"c03a895c-2d74-4d7f-891f-b752ce409b68": {
"match": "brand_token",
"title": "CLOPIDOGREL (CLOPIDOGREL BISULFATE) TABLET, FILM COATED [CARDINAL HEALTH 107, LLC]",
"spl_version": "3",
"published_date": "2026-04-30"
}
},
"productid": "71335-0581_71bf33e7-049d-4d2d-a83c-ed205142f17d",
"productndc": "71335-0581",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "202928",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "001",
"approval_date": "Feb 10, 2014"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CLOPIDOGREL BISULFATE",
"proprietary_name": "Clopidogrel",
"active_ingred_unit": "mg/1",
"application_number": "ANDA202928",
"marketing_category": "ANDA",
"nonproprietary_name": "Clopidogrel",
"start_marketing_date": "20121016",
"active_numerator_strength": "75"
}Related drugs
Other records sharing ATC code B01AC04.
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