fenofibrate
- Product NDC
- 69844-012
- 11-digit product format
- 698440012
- Labeler code
- 69844
- Product ID
- 69844-012_ef139fab-94f6-8568-e053-2a95a90a33bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Graviti Pharmaceuticals Private Limited
- Application
- ANDA211122
- Marketing category
- ANDA
- Marketing start
- 2020-03-18
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 48 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 69844-012-01 | 69844001201 | 30 TABLET in 1 BOTTLE (69844-012-01) | 30 tablet | 2020-03-18 | 0000-00-00 | No | No | Current |
| 69844-012-02 | 69844001202 | 90 TABLET in 1 BOTTLE (69844-012-02) | 90 tablet | 2020-03-18 | 0000-00-00 | No | No | Current |
| 69844-012-03 | 69844001203 | 1000 TABLET in 1 BOTTLE (69844-012-03) | 1000 tablet | 2020-03-18 | 0000-00-00 | No | No | Current |