NDC 51655-796
Buspirone Hydrochloride 10 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Strides Pharma Science Limited's NDC 64380-742.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Strides Pharma Science Limited names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA202330
- On the market since
- Feb 18, 2022
- Package NDCs
51655-796-26- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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