Fenofibrate
- Product NDC
- 16714-740
- 11-digit product format
- 167140740
- Labeler code
- 16714
- Product ID
- 16714-740_502bc6e9-5f21-4a1e-866d-baa8a08b512e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Northstar Rx LLC
- Application
- ANDA207378
- Marketing category
- ANDA
- Marketing start
- 2017-08-21
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 134 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 |
|---|
| 16714-740-01 | 16714074001 | 90 CAPSULE in 1 BOTTLE, PLASTIC (16714-740-01) | 90 capsule | 2017-08-21 | 0000-00-00 | No | No | Current |
| 16714-740-02 | 16714074002 | 100 CAPSULE in 1 BOTTLE, PLASTIC (16714-740-02) | 100 capsule | 2017-08-21 | 0000-00-00 | No | No | Current |