Gemfibrozil
- Product NDC
- 70518-1301
- 11-digit product format
- 705181301
- Labeler code
- 70518
- Product ID
- 70518-1301_91a10db7-8a64-4db1-e053-2a95a90ac179
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gemfibrozil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA077836
- Marketing category
- ANDA
- Marketing start
- 2018-07-12
- 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