NDC 70518-1981
Buspirone hydrochloride 30 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-183.
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
- 30 mg
- Approval
- ANDA ANDA078888
- On the market since
- Mar 26, 2019
- Package NDCs
70518-1981-070518-1981-170518-1981-270518-1981-3- Official label
- DailyMed (National Library of Medicine), updated Jan 22, 2025
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