Zydus Lifesciences Limited
Ahmedabad, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Aug 5, 2022. 10 inspections on record, 3 with serious problems.
NDC 72189-294
Memantine Hydrochloride 5 mg tablet
On the label: Direct Rx.
It's a repackaged product: Direct Rx rebottles it from Viona Pharmaceuticals Inc.'s NDC 72578-003.
Where the pills inside were made
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Product details
- Generic drug
- Memantine: see every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA090961
- On the market since
- Nov 11, 2021
- Package NDCs
72189-294-3072189-294-6072189-294-90- Official label
- DailyMed (National Library of Medicine), updated Mar 6, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?