NDC 68382-547
Memantine hydrochloride 14 mg capsule, extended release
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- capsule, extended release, oral
- Strength
- 14 mg
- Approval
- ANDA ANDA203293
- On the market since
- Apr 8, 2018
- Package NDCs
68382-547-0668382-547-1668382-547-3068382-547-77- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?