NDC 71335-0741 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0741
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076433
- Marketed since
- June 1, 2017
- 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 |
|---|---|---|
| 71335-0741-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0741-1) | Mar 16, 2018 |
| 71335-0741-2 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0741-2) | Mar 16, 2018 |
| 71335-0741-3 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0741-3) | Dec 27, 2021 |
| 71335-0741-4 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-0741-4) | Dec 27, 2021 |
| 71335-0741-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-0741-5) | Dec 27, 2021 |
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