NDC 68788-8647
Memantine Hydrochloride 10 mg tablet
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-071.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Chhatrapati Sambhajinagar, India | Makes it | Problems found, fixed voluntarilyApr 21, 2026 · 6 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Memantine: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA206528
- On the market since
- May 1, 2024
- Package NDCs
68788-8647-368788-8647-668788-8647-9- Official label
- DailyMed (National Library of Medicine), updated Jun 17, 2026
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