clopidogrel

Generic: clopidogrel bisulfate

Labeler: westminster pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name clopidogrel
Generic Name clopidogrel bisulfate
Labeler westminster pharmaceuticals, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

clopidogrel bisulfate 300 mg/1

Manufacturer
Westminster Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69367-194
Product ID 69367-194_175ba166-6dc4-41d9-a75e-853cb6d47aeb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204165
Listing Expiration 2026-12-31
Marketing Start 2018-07-27

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 69367194
Hyphenated Format 69367-194

Supplemental Identifiers

RxCUI
309362 749196
UPC
0369367194303
UNII
08I79HTP27

Packaging Origin

Original Packager
true

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 ANDA204165 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-05)
  • 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-30)
source: ndc

Packages (2)

69367-194-05 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-05) 69367-194-30 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-30)

Ingredients (1)

clopidogrel bisulfate (300 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": "175ba166-6dc4-41d9-a75e-853cb6d47aeb", "openfda": {"upc": ["0369367194303"], "unii": ["08I79HTP27"], "rxcui": ["309362", "749196"], "spl_set_id": ["bb3b5e96-e629-4db5-8ad5-40c17c6dae18"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-05)", "package_ndc": "69367-194-05", "marketing_start_date": "20180727"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-194-30)", "package_ndc": "69367-194-30", "marketing_start_date": "20180727"}], "brand_name": "Clopidogrel", "product_id": "69367-194_175ba166-6dc4-41d9-a75e-853cb6d47aeb", "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": "69367-194", "generic_name": "Clopidogrel Bisulfate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Clopidogrel", "active_ingredients": [{"name": "CLOPIDOGREL BISULFATE", "strength": "300 mg/1"}], "application_number": "ANDA204165", "marketing_category": "ANDA", "marketing_start_date": "20180727", "listing_expiration_date": "20261231"}