NDC 71335-0900 – Donepezil hydrochloride

Donepezil Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0900

Product details

Brand name
Donepezil hydrochloride
Generic name
Donepezil hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200292
Marketed since
November 1, 2011
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
71335-0900-130 TABLET, FILM COATED in 1 BOTTLE (71335-0900-1)Oct 1, 2019
71335-0900-260 TABLET, FILM COATED in 1 BOTTLE (71335-0900-2)Jan 28, 2022
71335-0900-390 TABLET, FILM COATED in 1 BOTTLE (71335-0900-3)Jul 12, 2018

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