NDC 33261-014
Buspirone Hydrochloride 10 mg tablet
On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-0054.
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.
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA075022
- On the market since
- Feb 28, 2002
- Package NDCs
33261-014-3033261-014-60- Official label
- DailyMed (National Library of Medicine), updated Sep 12, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?