NDC 68151-1993
Probenecid 500 mg tablet, film coated
On the label: Carilion Materials Management. It's repackaged from NDC 0378-0156, made by Mylan Pharmaceuticals Inc. (Probenecid). 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 Carilion Materials Management names for other drugs.
Product details
- Generic drug
- Probenecid: every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA084211
- On the market since
- Jan 13, 1976
- Package NDCs
68151-1993-0- Official label
- DailyMed (National Library of Medicine), updated Mar 9, 2006
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?