Memantine Hydrochloride 70771-1119
Product NDC
70771-1119- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 28, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA090961
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Memantine Hydrochloride | 5 mg/1 |
Drug Class
N-methyl-D-aspartate Receptor Antagonist [EPC]NMDA Receptor Antagonists [MoA]
Packaging Options(5)
1000 TABLET, FILM COATED in 1 BOTTLE (70771-1119-0)
100 TABLET, FILM COATED in 1 BOTTLE (70771-1119-1)
100 BLISTER PACK in 1 CARTON (70771-1119-4) / 1 TABLET, FILM COATED in 1 BLISTER PACK (70771-1119-2)
500 TABLET, FILM COATED in 1 BOTTLE (70771-1119-5)
60 TABLET, FILM COATED in 1 BOTTLE (70771-1119-6)