NDC 51655-015
Buspirone Hydrochloride 15 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-1003.
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 Teva Pharmaceuticals USA, Inc. 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
- 15 mg
- Approval
- ANDA ANDA075022
- On the market since
- Feb 25, 2015
- Package NDCs
51655-015-2651655-015-52- Official label
- DailyMed (National Library of Medicine), updated Dec 26, 2025
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