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
- 60290-078_54d2990d-e5aa-373e-e063-6294a90a4a98
- Product NDC
- 60290-078
- Form
- TABLET
- Composition / generic term
- VARENICLINE
- Labeler
- Umedica Laboratories USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260109
- Source listing expiry
- 20271231
Source-listed ingredients
- VARENICLINE TARTRATE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 56 TABLET in 1 BOTTLE (60290-078-01) · 60290-078-01
- 60 BLISTER PACK in 1 CARTON (60290-078-02) / 1 TABLET in 1 BLISTER PACK · 60290-078-02
- 56 TABLET in 1 BLISTER PACK (60290-078-03) · 60290-078-03
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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