NDC 62332-092 – Donepezil Hydrochloride

Donepezil Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC62332-092

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201724
Marketed since
January 29, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Donepezil Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
62332-092-10100 TABLET, FILM COATED in 1 CARTON (62332-092-10)Jan 29, 2016
62332-092-3030 TABLET, FILM COATED in 1 BOTTLE (62332-092-30)Jan 29, 2016
62332-092-9090 TABLET, FILM COATED in 1 BOTTLE (62332-092-90)Jan 29, 2016
62332-092-911000 TABLET, FILM COATED in 1 BOTTLE (62332-092-91)Jan 29, 2016

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