NDC 68788-8861 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8861
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA216798
- Marketed since
- April 11, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8861-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8861-3) | Apr 11, 2025 |
| 68788-8861-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8861-9) | Apr 11, 2025 |
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