NDC 71335-0891 – Fenofibrate
Fenofibrate 48 mg/1 · Tablet · Oral
Product NDC71335-0891
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208709
- Marketed since
- December 15, 2016
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 48 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0891-1 | 30 TABLET in 1 BOTTLE (71335-0891-1) | Apr 8, 2021 |
| 71335-0891-2 | 90 TABLET in 1 BOTTLE (71335-0891-2) | Jul 2, 2018 |
| 71335-0891-3 | 28 TABLET in 1 BOTTLE (71335-0891-3) | Dec 27, 2021 |
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