NDC 63629-8483 – Donepezil Hydrochloride

Donepezil Hydrochloride 23 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC63629-8483

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203104
Marketed since
March 1, 2015
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
63629-8483-130 TABLET, FILM COATED in 1 BOTTLE (63629-8483-1)May 18, 2021

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