ScieGen Pharmaceuticals, INC.
Hauppauge, NY, United States · makes it, tests it, packages it and labels it
Problems found, fixed voluntarily Last FDA inspection May 15, 2026. 15 inspections on record, 1 with serious problems.
NDC 50436-0325
Pregabalin 50 mg capsule
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Westminster Pharmaceuticals, LLC's NDC 69367-325.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Pregabalin: see every company that makes it
- Form
- capsule
- Strength
- 50 mg
- Approval
- ANDA ANDA208677
- On the market since
- Aug 24, 2021
- Package NDCs
50436-0325-150436-0325-250436-0325-3- Official label
- DailyMed (National Library of Medicine), updated Nov 5, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?