NDC 71335-2413 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet · Oral
Product NDC71335-2413
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA211122
- Marketed since
- July 18, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 145 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2413-1 | 30 TABLET in 1 BOTTLE (71335-2413-1) | Oct 11, 2024 |
| 71335-2413-2 | 90 TABLET in 1 BOTTLE (71335-2413-2) | May 29, 2024 |
| 71335-2413-3 | 28 TABLET in 1 BOTTLE (71335-2413-3) | Jan 31, 2025 |
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