NDC 70518-4392 – Donepezil Hydrochloride

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

Human Prescription Drug

Product NDC70518-4392

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090056
Marketed since
July 15, 2025
Listing expires
December 31, 2027
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
70518-4392-090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4392-0)Jul 15, 2025

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