NDC 0121-0646
Amantadine Hydrochloride 50 mg per 5 mL solution
On the label: Pharmaceutical Associates, Inc..
Where it's 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
- Jul 17, 1995
- Package NDCs
0121-0646-100121-0646-16- Official label
- DailyMed (National Library of Medicine), updated Aug 7, 2025
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