NDC 61442-192
Memantine Hydrochloride 5 mg tablet, film coated
On the label: Carlsbad Technology, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yiling Pharmaceutical Ltd | Shijiazhuang, China | Makes it | Serious problems, FDA actionOct 11, 2024 · 2 inspections, 1 with FDA action |
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA212947
- On the market since
- Jun 22, 2025
- Package NDCs
61442-192-0561442-192-60- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2025
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