GEMFIBROZIL
- Product NDC
- 60760-260
- 11-digit product format
- 607600260
- Labeler code
- 60760
- Product ID
- 60760-260_7a8ef282-d813-0ae9-e053-2991aa0ad812
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- GEMFIBROZIL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA078012
- Marketing category
- ANDA
- Marketing start
- 2017-12-15
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-260-60 | 60760026060 | 60 TABLET in 1 BOTTLE, PLASTIC (60760-260-60) | 60 tablet | 2017-12-15 | 0000-00-00 | No | No | Current |