Zydus Lifesciences Limited
Ahmedabad, India · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection Aug 5, 2022. 10 inspections on record, 3 with serious problems.
NDC 50436-0182
Buspirone hydrochloride 15 mg tablet
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-182.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Buspirone: see every company that makes it
- Form
- tablet
- Strength
- 15 mg
- Approval
- ANDA ANDA078888
- On the market since
- May 3, 2014
- Package NDCs
50436-0182-1- Official label
- DailyMed (National Library of Medicine), updated Sep 20, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?