NDC 60219-5522 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet · Oral
Product NDC60219-5522
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076509
- Marketed since
- June 22, 2022
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 60219-5522-5 | 500 TABLET in 1 BOTTLE (60219-5522-5) | Jun 22, 2022 |
| 60219-5522-9 | 90 TABLET in 1 BOTTLE (60219-5522-9) | Jun 22, 2022 |
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