NDC 61919-698
Nabumetone 750 mg tablet, film coated
On the label: Direct Rx. It's repackaged from NDC 68462-359, made by Glenmark Pharmaceuticals Inc., USA (Nabumetone). 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 Direct Rx names for other drugs.
Product details
- Generic drug
- Nabumetone: every company that makes it
- Form
- tablet, film coated
- Strength
- 750 mg
- Approval
- ANDA ANDA078671
- On the market since
- Aug 22, 2019
- Package NDCs
61919-698-60- Official label
- DailyMed (National Library of Medicine), updated Aug 22, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?