FENOFIBRATE
- Product NDC
- 50742-203
- 11-digit product format
- 507420203
- Labeler code
- 50742
- Product ID
- 50742-203_bd1b18a5-0a92-4214-9457-52fb0501e53e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA207564
- Marketing category
- ANDA
- Marketing start
- 2019-04-25
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 50742-203-01 | 50742020301 | 100 CAPSULE in 1 BOTTLE (50742-203-01) | 100 capsule | 2019-04-25 | 0000-00-00 | No | No | Current |
| 50742-203-05 | 50742020305 | 500 CAPSULE in 1 BOTTLE (50742-203-05) | 500 capsule | 2019-04-25 | 0000-00-00 | No | No | Current |