NDC 50090-4203
Memantine Hydrochloride 10 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 47335-322.
Where the pills inside were 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 |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, film coated
- Strength
- 10 mg
- Approval
- ANDA ANDA090058
- On the market since
- Jul 11, 2015
- Package NDCs
50090-4203-0- Official label
- DailyMed (National Library of Medicine), updated Nov 16, 2020
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