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
- 16714-052_dbf6d86e-5d4f-40da-a933-b928843053b7
- Product NDC
- 16714-052
- Form
- TABLET
- Composition / generic term
- Clopidogrel
- Labeler
- NorthStar RxLLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220809
- Source listing expiry
- 20261231
Source-listed ingredients
- CLOPIDOGREL BISULFATE — 75 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (16714-052-01) · 16714-052-01
- 90 TABLET in 1 BOTTLE (16714-052-02) · 16714-052-02
- 500 TABLET in 1 BOTTLE (16714-052-03) · 16714-052-03
- 1000 TABLET in 1 BOTTLE (16714-052-04) · 16714-052-04
- 10 TABLET in 1 BLISTER PACK (16714-052-10) · 16714-052-10
- 100 TABLET in 1 BOX, UNIT-DOSE (16714-052-11) · 16714-052-11
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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