NDC 68084-729 – Galantamine

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

Human Prescription Drug

Product NDC68084-729

Product details

Brand name
Galantamine
Generic name
Galantamine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090957
Marketed since
July 3, 2014
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Galantamine →

Package NDC codes (1)

Package NDCDescriptionSince
68084-729-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-729-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-729-11)Jul 3, 2014

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