Fenofibrate
- Product NDC
- 69367-269
- 11-digit product format
- 693670269
- Labeler code
- 69367
- Product ID
- 69367-269_9039dc84-8155-4561-b540-a5b28be598a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Westminster Pharmaceuticals, LLC
- Application
- ANDA207805
- Marketing category
- ANDA
- Marketing start
- 2020-11-20
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 69367-269-01 | 69367026901 | 100 CAPSULE in 1 BOTTLE (69367-269-01) | 100 capsule | 2020-11-20 | 0000-00-00 | No | No | Current |