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
- 42543-714_4b480542-0dd3-4694-9d43-d5fdcdd64a0f
- Product NDC
- 42543-714
- Form
- TABLET
- Composition / generic term
- clopidogrel
- Labeler
- Vensun Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141101
- Source listing expiry
- 20261231
Source-listed ingredients
- CLOPIDOGREL BISULFATE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (42543-714-01) · 42543-714-01
- 500 TABLET in 1 BOTTLE (42543-714-05) · 42543-714-05
- 30 TABLET in 1 BOTTLE (42543-714-30) · 42543-714-30
- 90 TABLET in 1 BOTTLE (42543-714-90) · 42543-714-90
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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