NDC 31722-596 – Fenofibrate
Fenofibrate 145 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-596
Product details
- Brand name
- Fenofibrate
- Generic name
- Fenofibrate
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA204598
- Marketed since
- July 14, 2016
- Listing expires
- December 31, 2026
- Pharmacologic class
- Peroxisome Proliferator Receptor alpha Agonist
Active ingredients
- Fenofibrate 145 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 31722-596-30 | 30 TABLET, FILM COATED in 1 BOTTLE (31722-596-30) | Jul 14, 2016 |
| 31722-596-31 | 70 TABLET, FILM COATED in 1 BLISTER PACK (31722-596-31) | Jul 14, 2016 |
| 31722-596-32 | 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-596-32) | Jul 14, 2016 |
| 31722-596-90 | 90 TABLET, FILM COATED in 1 BOTTLE (31722-596-90) | Jul 14, 2016 |
Recalls mentioning this NDC
- D-1211-2018 Oct 3, 2018 · Class III
Presence of Foreign Tablet/Capsule: A foreign identified as Valacyclovir tablet 500 mg was co-mingled in a bottle containing Fenofibrate Tablets, USP 145 mg.
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- 62332-351 Fenofibrate 160 mg/1 · Tablet, Film Coated · Alembic Pharmaceuticals Inc.