NDC 47335-322
Memantine Hydrochloride 10 mg tablet, film coated
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sun Pharmaceutical Industries Limited | Dadra, India | Makes it and tests it | Problems found, fixed voluntarilyMar 29, 2019 · 5 inspections |
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA090058
- On the market since
- Jul 11, 2015
- Package NDCs
47335-322-0847335-322-1347335-322-1847335-322-8347335-322-8647335-322-88- Official label
- DailyMed (National Library of Medicine), updated Oct 5, 2023
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