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United States · US · US:82009-021_e8fadba0-80b2-f6fd-ba68-512d796e5d89
Clopidogrel bisulfate
Orange BookUNIISPLATC B01AC04
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerQuallent Pharmaceuticals Health LLC
CountryUS (United States)
ATC codeB01AC04
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118200902105500 TABLET, FILM COATED in 1 BOTTLE (82009-021-05)
Annotations
UNII (FDA Substance ID)
08I79HTP27
CLOPIDOGREL BISULFATE
RxCUI 236991
Orange Book
A076273
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": "82009-021_e8fadba0-80b2-f6fd-ba68-512d796e5d89",
"productndc": "82009-021",
"dosage_form": "TABLET, FILM COATED",
"orange_book": {
"appl_no": "076273",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AB",
"strength": "EQ 75MG BASE",
"product_no": "001",
"approval_date": "Jan 14, 2008"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "CLOPIDOGREL BISULFATE",
"proprietary_name": "Clopidogrel bisulfate",
"active_ingred_unit": "mg/1",
"application_number": "ANDA076273",
"marketing_category": "ANDA",
"nonproprietary_name": "Clopidogrel bisulfate",
"start_marketing_date": "20221115",
"active_numerator_strength": "75"
}Related drugs
Other records sharing ATC code B01AC04.
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