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DONEPEZIL HYDROCHLORIDE

NDC 68180-527 · Lupin Pharmaceuticals, Inc.

Generic nameDONEPEZIL HYDROCHLORIDE
Dosage formTABLET
RouteORAL
Active ingredient(s)DONEPEZIL HYDROCHLORIDE
Strength23 mg/1
Pharmacologic classCholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
Marketing categoryANDA

Packages

68180-527-06 — 30 TABLET in 1 BOTTLE (68180-527-06)

68180-527-09 — 90 TABLET in 1 BOTTLE (68180-527-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62559-207 — MEMANTINE AND DONEPEZIL HYDROCHLORIDES, 62756-194 — Donepezil Hydrochloride, 62856-245 — donepezil hydrochloride, 62856-246 — donepezil hydrochloride, 62856-247 — donepezil hydrochloride, 63629-8483 — Donepezil Hydrochloride, 63629-9326 — Donepezil Hydrochloride, 65862-325 — Donepezil Hydrochloride, 65862-326 — Donepezil Hydrochloride, 67046-1476 — 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, 70518-1666 — donepezil hydrochloride, 70518-4380 — 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.