NDC 71335-2766 – Galantamine

Galantamine Hydrobromide 4 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2766

Product details

Brand name
Galantamine
Generic name
Galantamine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090957
Marketed since
March 29, 2011
Listing expires
December 31, 2027
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Galantamine →

Package NDC codes (2)

Package NDCDescriptionSince
71335-2766-160 TABLET, FILM COATED in 1 BOTTLE (71335-2766-1)Oct 3, 2025
71335-2766-290 TABLET, FILM COATED in 1 BOTTLE (71335-2766-2)Oct 3, 2025

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