NDC 71335-1908 – Memantine Hydrochloride
Memantine Hydrochloride 10 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1908
Product details
- Brand name
- Memantine Hydrochloride
- Generic name
- Memantine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090058
- Marketed since
- July 11, 2015
- Listing expires
- December 31, 2026
- Pharmacologic class
- N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Memantine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Memantine hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1908-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1908-1) | Jul 15, 2021 |
| 71335-1908-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1908-2) | Jul 15, 2021 |
| 71335-1908-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1908-3) | Jul 15, 2021 |
| 71335-1908-4 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-1908-4) | Jul 15, 2021 |
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