United States · FDA National Drug Code directory
Memantine Hydrochloride
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70771-1119_71694aca-1930-42bc-8322-6470fd047953
- Product NDC
- 70771-1119
- Form
- TABLET, FILM COATED
- Composition / generic term
- Memantine Hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170928
- Source listing expiry
- 20261231
Source-listed ingredients
- MEMANTINE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1119-0) · 70771-1119-0
- 100 TABLET, FILM COATED in 1 BOTTLE (70771-1119-1) · 70771-1119-1
- 100 BLISTER PACK in 1 CARTON (70771-1119-4) / 1 TABLET, FILM COATED in 1 BLISTER PACK (70771-1119-2) · 70771-1119-4
- 500 TABLET, FILM COATED in 1 BOTTLE (70771-1119-5) · 70771-1119-5
- 60 TABLET, FILM COATED in 1 BOTTLE (70771-1119-6) · 70771-1119-6
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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