NDC 42291-468
Furosemide 20 mg tablet
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-401.
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 Solco Healthcare U.S., LLC names for other drugs.
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA076796
- On the market since
- Jan 4, 2022
- Package NDCs
42291-468-0142291-468-1042291-468-90- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?