Bora Pharmaceuticals Inc.
Maple Grove, MN, United States · makes it, tests it and packages it
Problems found, fixed voluntarily Last FDA inspection Aug 30, 2022. 16 inspections on record.
NDC 0832-1112
Memantine Hydrochloride 5 mg tablet, film coated
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA090043
- On the market since
- Jul 31, 2015
- Package NDCs
0832-1112-60- Official label
- DailyMed (National Library of Medicine), updated Dec 11, 2025
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