NDC 48433-039 – Fenofibrate
Fenofibrate 48 mg/1 · Tablet, Film Coated · Oral
Product NDC48433-039
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Safecor Health, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA202856
- Marketed since
- March 17, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 48 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 48433-039-20 | 100 BLISTER PACK in 1 CARTON (48433-039-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-039-01) | Mar 17, 2026 |
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