NDC 68151-0910
Amantadine Hydrochloride 50 mg per 5 mL solution
On the label: Carilion Materials Management. It's repackaged: Carilion Materials Management 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 |
Repackaging site
- Carilion Materials Management, Roanoke, Virginia, United States · repackages it
Product details
- Generic drug
- Amantadine: every company that makes it
- Form
- solution
- Strength
- 50 mg per 5 mL
- Approval
- ANDA ANDA074509
- On the market since
- Jul 17, 1995
- Package NDCs
68151-0910-8- Official label
- DailyMed (National Library of Medicine), updated Aug 29, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?