NDC 67296-0691
Furosemide 20 mg tablet
On the label: RedPharm Drug. Inc.. It's repackaged from NDC 0378-0208, made by Mylan Pharmaceuticals 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 (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 RedPharm Drug. Inc. names for other drugs.
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- NDA NDA018487
- On the market since
- Aug 27, 1981
- Package NDCs
67296-0691-1- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?