FENOFIBRIC ACID
- Product NDC
- 50090-5369
- 11-digit product format
- 500905369
- Labeler code
- 50090
- Product ID
- 50090-5369_2abb54c6-1495-43f6-8755-402154a628f8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRIC ACID
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA212598
- Marketing category
- ANDA
- Marketing start
- 2019-07-25
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRIC ACID
- Active strength
- 135 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5369-0 | 50090536900 | 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-5369-0) | 2020-11-18 | 0000-00-00 | No | No | Current |