NDC 63629-5484
Oxybutynin Chloride 10 mg tablet, extended release
On the label: Bryant Ranch Prepack. It's repackaged from NDC 0093-5206, made by TEVA Pharmaceuticals USA Inc (Oxybutynin Chloride). 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 Bryant Ranch Prepack names for other drugs.
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet, extended release
- Strength
- 10 mg
- Approval
- ANDA ANDA076745
- On the market since
- May 11, 2007
- Package NDCs
63629-5484-1- Official label
- DailyMed (National Library of Medicine), updated Mar 20, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?