NDC 71335-1286 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet · Oral
Product NDC71335-1286
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210138
- Marketed since
- July 20, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1286-1 | 30 TABLET in 1 BOTTLE (71335-1286-1) | Sep 3, 2019 |
| 71335-1286-2 | 90 TABLET in 1 BOTTLE (71335-1286-2) | Aug 28, 2019 |
| 71335-1286-3 | 60 TABLET in 1 BOTTLE (71335-1286-3) | Dec 28, 2021 |
| 71335-1286-4 | 28 TABLET in 1 BOTTLE (71335-1286-4) | Dec 28, 2021 |
| 71335-1286-5 | 100 TABLET in 1 BOTTLE (71335-1286-5) | Dec 28, 2021 |
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