NDC 71205-948 – Donepezil Hydrochloride

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

Human Prescription Drug

Product NDC71205-948

Product details

Brand name
Donepezil Hydrochloride
Generic name
Donepezil Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203104
Marketed since
March 1, 2015
Listing expires
December 31, 2026
Pharmacologic class
Cholinesterase Inhibitor

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
71205-948-00100 TABLET, FILM COATED in 1 BOTTLE (71205-948-00)Nov 19, 2020
71205-948-3030 TABLET, FILM COATED in 1 BOTTLE (71205-948-30)Nov 19, 2020
71205-948-55500 TABLET, FILM COATED in 1 BOTTLE (71205-948-55)Nov 19, 2020
71205-948-6060 TABLET, FILM COATED in 1 BOTTLE (71205-948-60)Nov 19, 2020
71205-948-9090 TABLET, FILM COATED in 1 BOTTLE (71205-948-90)Nov 19, 2020

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