NDC 87063-305 – Donepezil hydrochloride

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

Human Prescription Drug

Product NDC87063-305

Product details

Brand name
Donepezil hydrochloride
Generic name
Donepezil hydrochloride
Labeler
ASCLEMED USA INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200292
Marketed since
November 1, 2011
Listing expires
December 31, 2027
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
87063-305-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-305-01)Sep 10, 2026
87063-305-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-305-20)Sep 10, 2026
87063-305-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-305-30)Sep 10, 2026
87063-305-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-305-60)Sep 10, 2026
87063-305-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-305-90)Sep 10, 2026

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