United States · FDA National Drug Code directory
Varenicline tartrate
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
- 71921-309_2b9c8b1e-6193-4d8e-9b50-6aca27294263
- Product NDC
- 71921-309
- Form
- TABLET, FILM COATED
- Composition / generic term
- Varenicline tartrate
- Labeler
- Florida Pharmaceutical Products, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241101
- Source listing expiry
- 20261231
Source-listed ingredients
- VARENICLINE TARTRATE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 56 TABLET, FILM COATED in 1 BOTTLE (71921-309-56) · 71921-309-56
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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