clopidogrel

Generic: clopidogrel bisulfate

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel bisulfate
Labeler golden state medical supply, inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 75 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-032
Product ID 51407-032_43fba049-b691-b443-e063-6394a90a4000
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076274
Listing Expiration 2026-12-31
Marketing Start 2012-05-17

Pharmacologic Class

Classes
cytochrome p450 2c8 inhibitors [moa] decreased platelet aggregation [pe] p2y12 platelet inhibitor [epc] p2y12 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51407032
Hyphenated Format 51407-032

Supplemental Identifiers

RxCUI
309362
UNII
08I79HTP27

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name clopidogrel (source: ndc)
Generic Name clopidogrel bisulfate (source: ndc)
Application Number ANDA076274 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 75 mg/1
source: ndc
Packaging
  • 1000 TABLET, FILM COATED in 1 BOTTLE (51407-032-10)
  • 30 TABLET, FILM COATED in 1 BOTTLE (51407-032-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (51407-032-90)
source: ndc

Packages (3)

51407-032-10 1000 TABLET, FILM COATED in 1 BOTTLE (51407-032-10) 51407-032-30 30 TABLET, FILM COATED in 1 BOTTLE (51407-032-30) 51407-032-90 90 TABLET, FILM COATED in 1 BOTTLE (51407-032-90)

Ingredients (1)

clopidogrel bisulfate (75 mg/1)

Linked Drug Pages (1)

Clopidogrel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "43fba049-b691-b443-e063-6394a90a4000", "openfda": {"unii": ["08I79HTP27"], "rxcui": ["309362"], "spl_set_id": ["84bb2c2c-4c41-4aa4-a52b-3d6eed794ada"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (51407-032-10)", "package_ndc": "51407-032-10", "marketing_start_date": "20180101"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51407-032-30)", "package_ndc": "51407-032-30", "marketing_start_date": "20180101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (51407-032-90)", "package_ndc": "51407-032-90", "marketing_start_date": "20180101"}], "brand_name": "Clopidogrel", "product_id": "51407-032_43fba049-b691-b443-e063-6394a90a4000", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cytochrome P450 2C8 Inhibitors [MoA]", "Decreased Platelet Aggregation [PE]", "P2Y12 Platelet Inhibitor [EPC]", "P2Y12 Receptor Antagonists [MoA]"], "product_ndc": "51407-032", "generic_name": "clopidogrel bisulfate", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "75 mg/1"}], "application_number": "ANDA076274", "marketing_category": "ANDA", "marketing_start_date": "20120517", "listing_expiration_date": "20261231"}