United States · FDA National Drug Code directory
Clopidogrel bisulfate
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
- 63739-178_2f97608b-b786-02f3-d5eb-5489e7069f8e
- Product NDC
- 63739-178
- Form
- TABLET, FILM COATED
- Composition / generic term
- Clopidogrel bisulfate
- Labeler
- McKesson Corporation dba SKY Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220818 / 20270731
Source-listed ingredients
- CLOPIDOGREL BISULFATE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 BLISTER PACK in 1 CARTON (63739-178-30) / 6 TABLET, FILM COATED in 1 BLISTER PACK · 63739-178-30
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →