NDC 51655-009 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet · Oral
Product NDC51655-009
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076509
- Marketed since
- May 7, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51655-009-52 | 30 TABLET in 1 BOTTLE, DISPENSING (51655-009-52) | May 7, 2014 |
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