NDC 47335-321 – Memantine Hydrochloride
Memantine Hydrochloride 5 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-321
Product details
- Brand name
- Memantine Hydrochloride
- Generic name
- Memantine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- 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 5 mg/1
Uses, dosage, side effects and warnings for Memantine hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 47335-321-08 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-321-08) | Jul 11, 2015 |
| 47335-321-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-321-18) | Jul 11, 2015 |
| 47335-321-86 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-321-86) | Jul 11, 2015 |
| 47335-321-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-321-88) | Jul 11, 2015 |
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