NDC 65862-459 – Galantamine

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

Human Prescription Drug

Product NDC65862-459

Product details

Brand name
Galantamine
Generic name
Galantamine
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090957
Marketed since
March 29, 2011
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Galantamine →

Package NDC codes (3)

Package NDCDescriptionSince
65862-459-6060 TABLET, FILM COATED in 1 BOTTLE (65862-459-60)Mar 29, 2011
65862-459-717000 TABLET, FILM COATED in 1 BOTTLE (65862-459-71)Mar 29, 2011
65862-459-991000 TABLET, FILM COATED in 1 BOTTLE (65862-459-99)Mar 29, 2011

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