Gemfibrozil
- Product NDC
- 0179-0221
- 11-digit product format
- 001790221
- Labeler code
- 0179
- Product ID
- 0179-0221_7bc086db-f5ef-9b82-e053-2a91aa0aecc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Gemfibrozil
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA077836
- Marketing category
- ANDA
- Marketing start
- 2016-11-29
- Marketing end
- 2020-04-30
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record