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Donepezil

NDC 60687-292 · American Health Packaging

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

Packages

60687-292-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-292-01) / 1 TABLET in 1 BLISTER PACK (60687-292-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6329 — Donepezil Hydrochloride, 50090-7365 — Donepezil Hydrochloride, 50228-139 — Donepezil Hydrochloride, 50228-140 — Donepezil Hydrochloride, 51407-320 — Donepezil Hydrochloride, 55111-302 — Donepezil hydrochloride, 55154-7882 — Donepezil Hydrochloride, 55154-7883 — Donepezil Hydrochloride, 60429-321 — Donepezil Hydrochloride, 60429-322 — Donepezil Hydrochloride, 60687-303 — Donepezil hydrochloride, 62332-092 — Donepezil Hydrochloride, 62332-093 — Donepezil Hydrochloride, 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, +70 more

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