NDC 63304-449 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral
Product NDC63304-449
Product details
- Brand name
- Fenofibrate
- Generic name
- fenofibrate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA200884
- Marketed since
- June 1, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 145 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 63304-449-05 | 500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05) | Jun 1, 2018 |
| 63304-449-30 | 30 TABLET, FILM COATED in 1 BOTTLE (63304-449-30) | Jun 1, 2018 |
| 63304-449-90 | 90 TABLET, FILM COATED in 1 BOTTLE (63304-449-90) | Jun 1, 2018 |
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