NDC 11819-282
Probenecid 500 mg tablet, film coated
On the label: HHS/Program Support Center/Supply Service Center. It's repackaged: HHS/Program Support Center/Supply Service Center rebottles it from Actavis Pharma, Inc.'s NDC 0591-5347.
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 Actavis Pharma, Inc. names for other drugs.
Product details
- Generic drug
- Probenecid: every company that makes it
- Form
- tablet, film coated
- Strength
- 500 mg
- Approval
- ANDA ANDA084442
- On the market since
- Jul 1, 1983
- Package NDCs
11819-282-08- Official label
- DailyMed (National Library of Medicine), updated Feb 29, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?