NDC 60687-797
Amantadine Hydrochloride 50 mg per 5 mL solution
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0646.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | Greenville, SC, United States | Makes it | No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action |
Product details
- Generic drug
- Amantadine: every company that makes it
- Form
- solution, oral
- Strength
- 50 mg per 5 mL
- Approval
- ANDA ANDA074509
- On the market since
- Feb 26, 2024
- Package NDCs
60687-797-4260687-797-4860687-797-56- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2024
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