NDC 47335-836 – Galantamine Hydrobromide

Galantamine Hydrobromide 16 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug

Product NDC47335-836

Product details

Brand name
Galantamine Hydrobromide
Generic name
Galantamine Hydrobromide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090178
Marketed since
February 9, 2011
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Galantamine Hydrobromide →

Package NDC codes (4)

Package NDCDescriptionSince
47335-836-08100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-08)Feb 9, 2011
47335-836-181000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-18)Feb 9, 2011
47335-836-8330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-83)Feb 9, 2011
47335-836-88100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-836-88)Feb 9, 2011

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