NDC 53746-173 – Memantine hydrochloride
Memantine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC53746-173
Product details
- Brand name
- Memantine hydrochloride
- Generic name
- Memantine
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090041
- Marketed since
- April 30, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Memantine Hydrochloride 5 mg/1
Uses, dosage, side effects and warnings for Memantine hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 53746-173-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (53746-173-10) | Apr 30, 2015 |
| 53746-173-30 | 30 TABLET, FILM COATED in 1 BOTTLE (53746-173-30) | Apr 30, 2015 |
| 53746-173-60 | 60 TABLET, FILM COATED in 1 BOTTLE (53746-173-60) | Apr 30, 2015 |
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