NDC 71335-3086 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-3086
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA216798
- Marketed since
- September 27, 2022
- 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 |
|---|---|---|
| 71335-3086-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-3086-1) | Feb 16, 2026 |
| 71335-3086-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-3086-2) | Feb 16, 2026 |
| 71335-3086-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-3086-3) | Feb 16, 2026 |
| 71335-3086-4 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-3086-4) | Feb 16, 2026 |
| 71335-3086-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-3086-5) | Feb 16, 2026 |
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