NDC 53002-5017
BusPIRone Hydrochloride 10 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Apnar Pharma LP's NDC 24689-907.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Inventia Healthcare Limited | Thane, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 12, 2025 · 4 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA209696
- On the market since
- Jul 3, 2018
- Package NDCs
53002-5017-053002-5017-353002-5017-6- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2020
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