NDC 54868-6455
Buspirone Hydrochloride 7.5 mg tablet
On the label: Physicians Total Care, Inc.. It's repackaged from NDC 49884-725, made by Par Pharmaceutical, Inc. (Buspirone Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). 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 Physicians Total Care, Inc. names for other drugs.
Product details
- Generic drug
- Buspirone: every company that makes it
- Form
- tablet
- Strength
- 7.5 mg
- Approval
- ANDA ANDA075467
- On the market since
- Apr 30, 2012
- Package NDCs
54868-6455-054868-6455-1- Official label
- DailyMed (National Library of Medicine), updated May 7, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?