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 50436-0727
Ranitidine 15 mg per 1 mL syrup
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0727.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Ranitidine: see every company that makes it
- Form
- syrup
- Strength
- 15 mg per 1 mL
- Approval
- ANDA ANDA077405
- On the market since
- Nov 1, 2010
- Package NDCs
50436-0727-1- Official label
- DailyMed (National Library of Medicine), updated May 24, 2018
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?