NDC 68788-8106 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8106
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204598
- Marketed since
- November 3, 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 |
|---|---|---|
| 68788-8106-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1) | Nov 3, 2021 |
| 68788-8106-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8106-3) | Nov 3, 2021 |
| 68788-8106-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8106-6) | Nov 3, 2021 |
| 68788-8106-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8106-9) | Nov 3, 2021 |
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