PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma
Greenville, SC, United States · makes it
No problems found Last FDA inspection Aug 1, 2025. 18 inspections on record, 1 with serious problems.
NDC 50436-0646
Amantadine Hydrochloride 50 mg per 5 mL solution
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0646.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Amantadine: see 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
50436-0646-1- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2018
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