NDC 71205-949 – Fenofibrate
Fenofibrate 160 mg/1 · Tablet, Film Coated · Oral
Product NDC71205-949
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Proficient Rx LP
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA207803
- Marketed since
- April 23, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 160 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71205-949-30 | 30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30) | Oct 8, 2020 |
| 71205-949-55 | 500 TABLET, FILM COATED in 1 BOTTLE (71205-949-55) | Oct 8, 2020 |
| 71205-949-60 | 60 TABLET, FILM COATED in 1 BOTTLE (71205-949-60) | Oct 8, 2020 |
| 71205-949-72 | 120 TABLET, FILM COATED in 1 BOTTLE (71205-949-72) | Oct 8, 2020 |
| 71205-949-78 | 180 TABLET, FILM COATED in 1 BOTTLE (71205-949-78) | Oct 8, 2020 |
| 71205-949-90 | 90 TABLET, FILM COATED in 1 BOTTLE (71205-949-90) | Oct 8, 2020 |
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