Class II ยท Moderate risk
rifAXIMin Tablet
Labeling:Label Mixup; rifAXIMin Tablet, 200 mg may be potentially mislabeled as CapsuleTOPRIL, Tablet, 25 mg, NDC 00143117201, Pedigree: AD52778_19, EXP: 5/20/2014.
National Drug Code
Is NDC 65649-0301-03 recalled?
Xifaxan · 30 TABLET in 1 BOTTLE (65649-301-03)
Yes — this exact package was recalled
1 FDA recall names the code 65649-0301-03 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
- rifaximin
- Strength
- RIFAXIMIN 200 mg/1
- Form
- Tablet · Oral
- Labeler
- Salix Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 65649-0301
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.
Free recall alerts
Know the day your medication is recalled
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