NDC 70436-005 – Galantamine

Galantamine Hydrobromide 8 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70436-005

Product details

Brand name
Galantamine
Generic name
Galantamine
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077604
Marketed since
August 2, 2017
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
70436-005-0660 TABLET, FILM COATED in 1 BOTTLE (70436-005-06)Aug 2, 2017

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