Class II ยท Moderate risk
RIVAROXABAN Tablet
Labeling: Label Mixup; RIVAROXABAN Tablet, 20 mg may be potentially mislabeled as VENLAFAXINE HCL, Tablet, 100 mg, NDC 00093738301, Pedigree: W002619, EXP: 6/4/2014.
National Drug Code
Is NDC 50458-0579-30 recalled?
Xarelto · 30 TABLET, FILM COATED in 1 BOTTLE (50458-579-30)
Yes — this exact package was recalled
1 FDA recall names the code 50458-0579-30 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
- rivaroxaban
- Strength
- RIVAROXABAN 20 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Janssen Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 50458-0579
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
- 50458-0176 See recall 1
- 50458-0178 See recall 1
- 50458-0196 See recall 1
- 50458-0306 Risperdal Consta 1
- 50458-0543 Invokamet 1
- 50458-0578 Xarelto 1
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