NDC 71335-1732 – Memantine Hydrochloride
Memantine Hydrochloride 5 mg/1 · Tablet · Oral
Product NDC71335-1732
Product details
- Brand name
- Memantine Hydrochloride
- Generic name
- Memantine Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090961
- Marketed since
- February 28, 2019
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1732-1 | 30 TABLET in 1 BOTTLE (71335-1732-1) | Nov 11, 2020 |
| 71335-1732-2 | 60 TABLET in 1 BOTTLE (71335-1732-2) | Nov 11, 2020 |
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