United States · FDA National Drug Code directory
Clopidogrel
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 69367-200_175ba166-6dc4-41d9-a75e-853cb6d47aeb
- Product NDC
- 69367-200
- Form
- TABLET, FILM COATED
- Composition / generic term
- Clopidogrel Bisulfate
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230515
- Source listing expiry
- 20261231
Source-listed ingredients
- CLOPIDOGREL BISULFATE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-200-05) · 69367-200-05
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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