NDC 0904-6734 – Memantine hydrochloride
Memantine Hydrochloride 7 mg/1 · Capsule, Extended Release · Oral
Product NDC0904-6734
Product details
- Brand name
- Memantine hydrochloride
- Generic name
- Memantine hydrochloride
- Labeler
- Major Pharmaceuticals
- Dosage form
- Capsule, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA206028
- Marketed since
- February 20, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Memantine Hydrochloride 7 mg/1
Uses, dosage, side effects and warnings for Memantine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0904-6734-61 | 100 BLISTER PACK in 1 CARTON (0904-6734-61) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK | Feb 20, 2018 |
Recalls mentioning this NDC
- D-0485-2026 Apr 22, 2026 · Class II
Failed Dissolution Specifications - D-1262-2020 May 20, 2020 · Class III
Failed dissolution specifications: Low stage 3 results obtained for dissolution during routine stability testing. - D-0844-2020 Feb 26, 2020 · Class III
Failed Dissolution Specifications: High out of specification result observed at stability studies.
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- 59651-404 Memantine Hydrochloride 7 mg/1 · Capsule, Extended Release · Aurobindo Pharma Limited
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- 68180-249 Memantine Hydrochloride 28 mg/1 · Capsule, Extended Release · Lupin Pharmaceuticals, Inc.
- 68180-248 Memantine Hydrochloride 21 mg/1 · Capsule, Extended Release · Lupin Pharmaceuticals, Inc.
- 68180-246 Memantine Hydrochloride 7 mg/1 · Capsule, Extended Release · Lupin Pharmaceuticals, Inc.
- 68180-247 Memantine Hydrochloride 14 mg/1 · Capsule, Extended Release · Lupin Pharmaceuticals, Inc.