United States · FDA National Drug Code directory
varenicline
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
- 75834-335_077ec752-4145-4592-9ee1-6fdc9a04795a
- Product NDC
- 75834-335
- Form
- TABLET, FILM COATED
- Composition / generic term
- varenicline
- Labeler
- Nivagen Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260302
- Source listing expiry
- 20271231
Source-listed ingredients
- VARENICLINE TARTRATE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 BLISTER PACK in 1 CARTON (75834-335-27) / 14 TABLET, FILM COATED in 1 BLISTER PACK · 75834-335-27
- 56 TABLET, FILM COATED in 1 BOTTLE (75834-335-28) · 75834-335-28
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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