NDC 61919-600
Buspirone Hydrochloride 10 mg tablet
On the label: Direct Rx. It's repackaged: Direct Rx rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-181.
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 |
Repackaging site
- Direct Rx, Dawsonville, GA, United States · repackages it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA078888
- On the market since
- Jan 1, 2015
- Package NDCs
61919-600-90- Official label
- DailyMed (National Library of Medicine), updated Oct 28, 2015
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