NDC 51655-433 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-433
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200884
- Marketed since
- September 17, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 145 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51655-433-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-433-52) | Sep 17, 2020 |
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