NDC 35561-250 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral
Product NDC35561-250
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Bostal LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208476
- Marketed since
- January 1, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 145 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 35561-250-03 | 500 TABLET, FILM COATED in 1 BOTTLE (35561-250-03) | Aug 7, 2025 |
| 35561-250-10 | 30 TABLET, FILM COATED in 1 BOTTLE (35561-250-10) | Jan 1, 2021 |
| 35561-250-11 | 90 TABLET, FILM COATED in 1 BOTTLE (35561-250-11) | Aug 15, 2025 |
| 35561-250-13 | 500 TABLET, FILM COATED in 1 BOTTLE (35561-250-13) | Jan 1, 2021 |
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