Fenofibric Acid
- Product NDC
- 10370-210
- 11-digit product format
- 103700210
- Labeler code
- 10370
- Product ID
- 10370-210_3bb9dd8f-77dc-45ae-9c13-9c6e8f8f5f1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibric Acid
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Par Pharmaceutical, Inc.
- Application
- ANDA201573
- Marketing category
- ANDA
- Marketing start
- 2013-07-18
- Marketing end
- 2021-07-31
- Substance
- CHOLINE FENOFIBRATE
- Active strength
- 135 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10370-210-09 | 10370021009 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (10370-210-09) | 2013-07-18 | 2021-07-31 | No | No | Current |