Memantine Hydrochloride 47335-0321
Product NDC
47335-0321- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 11, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA090058
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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(4)
100 TABLET, FILM COATED in 1 BOTTLE (47335-321-08)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-321-18)
60 TABLET, FILM COATED in 1 BOTTLE (47335-321-86)
100 TABLET, FILM COATED in 1 BOTTLE (47335-321-88)