NDC 24979-722 – Galantamine

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

Human Prescription Drug

Product NDC24979-722

Product details

Brand name
Galantamine
Generic name
galantamine
Labeler
Upsher-Smith Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077604
Marketed since
March 6, 2024
Listing expires
December 31, 2027
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Galantamine →

Package NDC codes (1)

Package NDCDescriptionSince
24979-722-0460 TABLET, FILM COATED in 1 BOTTLE (24979-722-04)Mar 6, 2024

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