NDC 33342-061 – Donepezil Hydrochloride

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

Human Prescription Drug

Product NDC33342-061

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202631
Marketed since
January 23, 2014
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
33342-061-0730 TABLET, FILM COATED in 1 BOTTLE (33342-061-07)Jan 23, 2014
33342-061-1090 TABLET, FILM COATED in 1 BOTTLE (33342-061-10)Jan 23, 2014
33342-061-1210 BLISTER PACK in 1 CARTON (33342-061-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKJan 23, 2014

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