NDC 21695-406
Oxybutynin Chloride 5 mg tablet
On the label: Rebel Distributors Corp... It's repackaged from NDC 0603-4975, made by Par Pharmaceutical, 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. 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 Rebel Distributors Corp.. names for other drugs.
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet
- Strength
- 5 mg
- Approval
- ANDA ANDA075079
- On the market since
- Oct 31, 1997
- Package NDCs
21695-406-30- Official label
- DailyMed (National Library of Medicine), updated Sep 4, 2009
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?