NDC 67046-221
Furosemide 40 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 0172-2907, made by Teva Pharmaceuticals USA, Inc. (Furosemide). 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
- Furosemide: every company that makes it
- Form
- tablet
- Strength
- 40 mg
- Approval
- ANDA ANDA018413
- On the market since
- Feb 8, 2011
- Package NDCs
67046-221-30- Official label
- DailyMed (National Library of Medicine), updated Dec 9, 2010
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