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
- 82804-986_330702d9-842c-416d-9b11-b4a9b707e9b2
- Product NDC
- 82804-986
- Form
- TABLET, FILM COATED
- Composition / generic term
- Clopidogrel Bisulfate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180727
- 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, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-00) · 82804-986-00
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-30) · 82804-986-30
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-55) · 82804-986-55
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-60) · 82804-986-60
- 240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-64) · 82804-986-64
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-72) · 82804-986-72
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-78) · 82804-986-78
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-90) · 82804-986-90
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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