NDC 33342-028 – Donepezil Hydrochloride

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

Human Prescription Drug

Product NDC33342-028

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201146
Marketed since
August 17, 2012
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
33342-028-0730 TABLET, FILM COATED in 1 BOTTLE (33342-028-07)Aug 17, 2012
33342-028-1090 TABLET, FILM COATED in 1 BOTTLE (33342-028-10)Aug 17, 2012
33342-028-1210 BLISTER PACK in 1 CARTON (33342-028-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKAug 17, 2012
33342-028-15500 TABLET, FILM COATED in 1 BOTTLE (33342-028-15)Nov 6, 2014
33342-028-315 BLISTER PACK in 1 CARTON (33342-028-31) / 10 TABLET, FILM COATED in 1 BLISTER PACKAug 17, 2012
33342-028-441000 TABLET, FILM COATED in 1 BOTTLE (33342-028-44)Nov 6, 2014

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