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DONEPEZIL HYDROCHLORIDE

NDC 72189-031 · Direct_Rx

Generic nameDONEPEZIL HYDROCHLORIDE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)DONEPEZIL HYDROCHLORIDE
Strength5 mg/1
Pharmacologic classCholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
Marketing categoryANDA

Packages

72189-031-30 — 30 TABLET, FILM COATED in 1 BOTTLE (72189-031-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4392 — Donepezil Hydrochloride, 71093-127 — Donepezil Hydrochloride, 71093-128 — Donepezil Hydrochloride, 71205-948 — Donepezil Hydrochloride, 71209-019 — donepezil hydrochloride, 71209-020 — donepezil hydrochloride, 71335-0416 — Donepezil Hydrochloride, 71335-0900 — donepezil hydrochloride, 71335-2022 — Donepezil Hydrochloride, 71335-2065 — Donepezil Hydrochloride, 71335-2093 — Donepezil Hydrochloride, 71335-2346 — Donepezil Hydrochloride, 71335-2436 — Donepezil Hydrochloride, 72162-1276 — Donepezil Hydrochloride, 72162-2136 — Donepezil Hydrochloride, 72162-2137 — Donepezil Hydrochloride, 72189-265 — DONEPEZIL HYDROCHLORIDE, 73190-004 — Memantine and Donepezil, 82009-119 — Donepezil hydrochloride, 82009-120 — Donepezil hydrochloride, +70 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.