NDC 46708-295 – Donepezil Hydrochloride

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

Human Prescription Drug

Product NDC46708-295

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201724
Marketed since
January 29, 2016
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
46708-295-10100 TABLET, FILM COATED in 1 CARTON (46708-295-10)Jan 29, 2016
46708-295-3030 TABLET, FILM COATED in 1 BOTTLE (46708-295-30)Jan 29, 2016
46708-295-9090 TABLET, FILM COATED in 1 BOTTLE (46708-295-90)Jan 29, 2016
46708-295-911000 TABLET, FILM COATED in 1 BOTTLE (46708-295-91)Jan 29, 2016

Other Donepezil Hydrochloride products