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Memantine Hydrochloride

NDC 70436-054 · Slate Run Pharmaceuticals, LLC

Generic namememantine hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)MEMANTINE HYDROCHLORIDE
Strength7 mg/1
Pharmacologic classN-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

70436-054-04 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-054-04)

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, 69680-161 — memantine hydrochloride, 69680-162 — memantine hydrochloride, 69680-163 — memantine hydrochloride, 69680-164 — memantine hydrochloride, 69680-183 — memantine hydrochloride and donepezil hydrochloride, 69680-185 — memantine hydrochloride and donepezil hydrochloride, 70436-055 — memantine hydrochloride, 70436-056 — memantine hydrochloride, 70436-057 — memantine hydrochloride, 70518-3338 — Memantine Hydrochloride, 70771-1119 — Memantine Hydrochloride, 70771-1120 — Memantine Hydrochloride, 70771-1321 — Memantine hydrochloride, 70771-1322 — Memantine hydrochloride, 70771-1323 — Memantine hydrochloride, 70771-1324 — Memantine hydrochloride, +115 more

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