Class III ยท Low risk
Fenofibrate Tablets
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.
National Drug Code
Is NDC 31722-0596-90 recalled?
Fenofibrate · 90 TABLET, FILM COATED in 1 BOTTLE (31722-596-90)
Yes — this exact package was recalled
1 FDA recall names the code 31722-0596-90 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Fenofibrate
- Strength
- FENOFIBRATE 145 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 31722-0596
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
- 31722-0726 Montelukast Sodium 3
- 31722-0713 Pantoprazole Sodium 2
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
Free recall alerts
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