GEMFIBROZIL
- Product NDC
- 68071-4011
- 11-digit product format
- 680714011
- Labeler code
- 68071
- Product ID
- 68071-4011_94e59c29-262b-c9ba-e053-2a95a90a4e73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GEMFIBROZIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA077836
- Marketing category
- ANDA
- Marketing start
- 2017-03-23
- Marketing end
- 0000-00-00
- Substance
- GEMFIBROZIL
- Active strength
- 600 mg/1
- Pharmacologic classes
- Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record