NDC 0832-1113
Memantine Hydrochloride 10 mg tablet, film coated
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bora Pharmaceuticals Inc. | Maple Grove, MN, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections |
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA090043
- On the market since
- Jul 31, 2015
- Package NDCs
0832-1113-60- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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