NDC 53217-276
Buspirone hydrochloride 5 mg tablet
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-180.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet
- Strength
- 5 mg
- Approval
- ANDA ANDA078888
- On the market since
- May 3, 2014
- Package NDCs
53217-276-3053217-276-60- Official label
- DailyMed (National Library of Medicine), updated Apr 20, 2017
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