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Donepezil Hydrochloride

NDC 46708-295 · Alembic Pharmaceuticals Limited

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

46708-295-10 — 100 TABLET, FILM COATED in 1 CARTON (46708-295-10)

46708-295-30 — 30 TABLET, FILM COATED in 1 BOTTLE (46708-295-30)

46708-295-90 — 90 TABLET, FILM COATED in 1 BOTTLE (46708-295-90)

46708-295-91 — 1000 TABLET, FILM COATED in 1 BOTTLE (46708-295-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

33342-029 — Donepezil Hydrochloride, 33342-030 — Donepezil Hydrochloride, 33342-061 — Donepezil Hydrochloride, 33342-312 — Memantine and Donepezil, 33342-313 — Memantine and Donepezil, 42799-954 — Donepezil hydrochloride, 43547-275 — donepezil hydrochloride, 43547-276 — donepezil hydrochloride, 43547-878 — donepezil hydrochloride, 43547-879 — donepezil hydrochloride, 46708-296 — Donepezil Hydrochloride, 50090-2627 — Donepezil hydrochloride, 50090-3537 — donepezil hydrochloride, 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, +70 more

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