NDC 68071-3542 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3542
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA216798
- Marketed since
- September 27, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3542-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3542-9) | Nov 29, 2023 |
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