NDC 70518-3338
Memantine Hydrochloride 5 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-003.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA090961
- On the market since
- Jan 20, 2022
- Package NDCs
70518-3338-070518-3338-170518-3338-2- Official label
- DailyMed (National Library of Medicine), updated Aug 6, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?