NDC 42385-935 – Fenofibrate
Fenofibrate 54 mg/1 · Tablet, Film Coated · Oral
Product NDC42385-935
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Laurus Labs Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA210606
- Marketed since
- January 13, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 54 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 42385-935-05 | 500 TABLET, FILM COATED in 1 BOTTLE (42385-935-05) | Jan 13, 2020 |
| 42385-935-11 | 1000 TABLET, FILM COATED in 1 BOTTLE (42385-935-11) | Jan 13, 2020 |
| 42385-935-30 | 30 TABLET, FILM COATED in 1 BOTTLE (42385-935-30) | Jan 13, 2020 |
| 42385-935-90 | 90 TABLET, FILM COATED in 1 BOTTLE (42385-935-90) | Jan 13, 2020 |
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