NDC 33342-219
Memantine hydrochloride 7 mg capsule, extended release
On the label: Macleods Pharmaceuticals Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Macleods Pharmaceuticals Limited | District Solan, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 6 inspections, 2 with FDA action |
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 7 mg
- Approval
- ANDA ANDA206310
- On the market since
- Aug 28, 2025
- Package NDCs
33342-219-0733342-219-12- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2025
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