NDC 33358-536
Pantoprazole Sodium 20 mg tablet, delayed release
On the label: RxChange Co.. It's repackaged from NDC 0093-0011, made by Teva Pharmaceuticals USA, Inc. (Pantoprazole Sodium). 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). 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 RxChange Co. names for other drugs.
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release
- Strength
- 20 mg
- Approval
- ANDA ANDA077056
- On the market since
- Dec 21, 2007
- Package NDCs
33358-536-60- Official label
- DailyMed (National Library of Medicine), updated Dec 2, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?