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United States · US · US:55154-2149_f2c8b1d7-dfbb-488c-b554-3b2d685fd6b6
Clopidogrel
Orange BookUNIISPLATC B01AC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCardinal Health 107, LLC
CountryUS (United States)
ATC codeB01AC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11551542149010 BLISTER PACK in 1 BAG (55154-2149-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
08I79HTP27
CLOPIDOGREL BISULFATE
RxCUI 236991
Orange Book
A076274
ABAB
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": "55154-2149_f2c8b1d7-dfbb-488c-b554-3b2d685fd6b6",
"productndc": "55154-2149",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "076274",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "001",
"approval_date": "May 17, 2012"
},
{
"rs": true,
"rld": false,
"te_code": "AB",
"strength": "EQ 300MG BASE",
"product_no": "002",
"approval_date": "Mar 4, 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": "ANDA076274",
"marketing_category": "ANDA",
"nonproprietary_name": "Clopidogrel Bisulfate",
"start_marketing_date": "20251010",
"active_numerator_strength": "75"
}Related drugs
Other records sharing ATC code B01AC04.
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