NDC 68788-8208 – Donepezil Hydrochloride

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

Human Prescription Drug

Product NDC68788-8208

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090056
Marketed since
June 3, 2022
Listing expires
December 31, 2027
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
68788-8208-330 TABLET, FILM COATED in 1 BOTTLE (68788-8208-3)Jun 3, 2022
68788-8208-660 TABLET, FILM COATED in 1 BOTTLE (68788-8208-6)Jun 3, 2022
68788-8208-990 TABLET, FILM COATED in 1 BOTTLE (68788-8208-9)Jun 3, 2022

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