NDC 71335-2016 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2016
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202856
- Marketed since
- May 14, 2013
- 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 |
|---|---|---|
| 71335-2016-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2016-1) | Feb 10, 2022 |
| 71335-2016-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2016-2) | Feb 10, 2022 |
| 71335-2016-3 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-2016-3) | Feb 10, 2022 |
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