NDC 33358-251
Nabumetone 500 mg tablet, film coated
On the label: RxChange Co.. It's repackaged from NDC 68462-358, 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 RxChange Co. names for other drugs.
Product details
- Generic drug
- Nabumetone: every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA078671
- On the market since
- Nov 13, 2014
- Package NDCs
33358-251-60- Official label
- DailyMed (National Library of Medicine), updated Nov 13, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?