NDC 51138-588
Gemfibrozil 600 mg tablet, film coated
On the label: Med Health Pharma, LLC. It's repackaged: Med Health Pharma, LLC rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9130.
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 Hikma Pharmaceuticals USA Inc. names for other drugs.
Product details
- Generic drug
- Gemfibrozil: every company that makes it
- Form
- tablet, film coated
- Strength
- 600 mg
- Approval
- ANDA ANDA077836
- On the market since
- Jul 4, 2011
- Package NDCs
51138-588-30- Official label
- DailyMed (National Library of Medicine), updated Jul 4, 2011
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?