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
- 43598-907_65233c50-9a25-15c3-cc2b-98713a8173b2
- Product NDC
- 43598-907
- Form
- TABLET, FILM COATED
- Composition / generic term
- varenicline tartrate
- Labeler
- Dr. Reddys Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241213
- Source listing expiry
- 20261231
Source-listed ingredients
- VARENICLINE TARTRATE — .5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 56 TABLET, FILM COATED in 1 BOTTLE (43598-907-56) · 43598-907-56
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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