NDC 71335-1756 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet · Oral
Product NDC71335-1756
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA213864
- Marketed since
- September 10, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1756-1 | 30 TABLET in 1 BOTTLE (71335-1756-1) | Dec 20, 2021 |
| 71335-1756-2 | 90 TABLET in 1 BOTTLE (71335-1756-2) | Dec 20, 2021 |
| 71335-1756-3 | 60 TABLET in 1 BOTTLE (71335-1756-3) | Dec 20, 2021 |
| 71335-1756-4 | 28 TABLET in 1 BOTTLE (71335-1756-4) | Dec 20, 2021 |
| 71335-1756-5 | 100 TABLET in 1 BOTTLE (71335-1756-5) | Dec 20, 2021 |
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