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
- 13668-141_3cbfb162-4652-4a90-9afa-489e743fc16a
- Product NDC
- 13668-141
- Form
- TABLET, FILM COATED
- Composition / generic term
- Clopidogrel
- Labeler
- Torrent Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120517
- Source listing expiry
- 20261231
Source-listed ingredients
- CLOPIDOGREL BISULFATE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (13668-141-01) · 13668-141-01
- 500 TABLET, FILM COATED in 1 BOTTLE (13668-141-05) · 13668-141-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (13668-141-10) · 13668-141-10
- 30 TABLET, FILM COATED in 1 BOTTLE (13668-141-30) · 13668-141-30
- 3100 TABLET, FILM COATED in 1 BOTTLE (13668-141-44) · 13668-141-44
- 90 TABLET, FILM COATED in 1 BOTTLE (13668-141-90) · 13668-141-90
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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