NDC 67046-535
Pantoprazole SodiumDelayed-Release 40 mg tablet, delayed release
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 0008-0607, made by Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer 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. 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 Coupler Enterprises Inc. names for other drugs.
Product details
- Generic drug
- Pantoprazole: every company that makes it
- Form
- tablet, delayed release
- Strength
- 40 mg
- Approval
- NDA NDA020987
- On the market since
- Feb 26, 2010
- Package NDCs
67046-535-30- Official label
- DailyMed (National Library of Medicine), updated Mar 31, 2009
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