NDC 70771-1322 – Memantine hydrochloride
Memantine Hydrochloride 14 mg/1 · Capsule, Extended Release · Oral
Product NDC70771-1322
Product details
- Brand name
- Memantine hydrochloride
- Generic name
- Memantine hydrochloride
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA203293
- Marketed since
- April 8, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Memantine Hydrochloride 14 mg/1
Uses, dosage, side effects and warnings for Memantine hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1322-3 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1322-3) | Apr 8, 2018 |
| 70771-1322-4 | 10 BLISTER PACK in 1 CARTON (70771-1322-4) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1322-2) | Apr 8, 2018 |
| 70771-1322-9 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1322-9) | Apr 8, 2018 |
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