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
- 65862-357_ff58c1f3-4875-4d10-aca7-c622af163cef
- Product NDC
- 65862-357
- Form
- TABLET, FILM COATED
- Composition / generic term
- Clopidogrel Bisulfate
- Labeler
- Aurobindo Pharma 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 (65862-357-01) · 65862-357-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-357-05) · 65862-357-05
- 10 BLISTER PACK in 1 CARTON (65862-357-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 65862-357-10
- 30 TABLET, FILM COATED in 1 BOTTLE (65862-357-30) · 65862-357-30
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-357-90) · 65862-357-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-357-99) · 65862-357-99
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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