NDC 51655-234 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet · Oral
Product NDC51655-234
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208709
- Marketed since
- August 16, 2022
- 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 |
|---|---|---|
| 51655-234-52 | 30 TABLET in 1 BOTTLE, PLASTIC (51655-234-52) | Aug 16, 2022 |
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