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donepezil hydrochloride

NDC 70518-1666 · REMEDYREPACK INC.

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

Packages

70518-1666-0 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1666-0)

70518-1666-1 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1666-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1476 — Donepezil Hydrochloride, 68180-527 — DONEPEZIL HYDROCHLORIDE, 68788-8208 — Donepezil Hydrochloride, 68788-8711 — Donepezil Hydrochloride, 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, 70518-4380 — Donepezil hydrochloride, 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, +70 more

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