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Donepezil Hydrochloride

NDC 71093-128 · ACI Healthcare USA, Inc.

Generic nameDonepezil Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)DONEPEZIL HYDROCHLORIDE
Strength10 mg/1
Pharmacologic classCholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
Marketing categoryANDA

Packages

71093-128-01 — 30 TABLET in 1 BOTTLE (71093-128-01)

71093-128-03 — 90 TABLET in 1 BOTTLE (71093-128-03)

71093-128-05 — 500 TABLET in 1 BOTTLE (71093-128-05)

71093-128-06 — 1000 TABLET in 1 BOTTLE (71093-128-06)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69238-1247 — Memantine and Donepezil, 69238-1248 — Memantine and Donepezil, 69238-1552 — Memantine and Donepezil, 69238-1553 — Memantine and Donepezil, 69680-183 — memantine hydrochloride and donepezil hydrochloride, 69680-185 — memantine hydrochloride and donepezil hydrochloride, 70518-1666 — donepezil hydrochloride, 70518-4380 — Donepezil hydrochloride, 70518-4392 — Donepezil Hydrochloride, 71093-127 — 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, +70 more

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