NDC 70710-1613 – Varenicline

Varenicline Tartrate .5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70710-1613

Product details

Brand name
Varenicline
Generic name
Varenicline
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216723
Marketed since
June 13, 2023
Listing expires
December 31, 2026
Pharmacologic class
Cholinergic Receptor Agonist; Partial Cholinergic Nicotinic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Varenicline →

Package NDC codes (1)

Package NDCDescriptionSince
70710-1613-656 TABLET, FILM COATED in 1 BOTTLE (70710-1613-6)Jun 13, 2023

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