Class II · Moderate risk
Risperdal CONSTA
Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA (risperiDONE) due to a sterility failure in a stability sample
National Drug Code
Is NDC 50458-0306-11 recalled?
Risperdal Consta · 1 KIT in 1 BOX (50458-306-11) * 2 mL in 1 SYRINGE (50458-306-01) * 2 mL in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 50458-0306-11 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
- risperidone
- Form
- Kit
- Labeler
- Janssen Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 50458-0306
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
- 50458-0543 Invokamet 1
- 50458-0578 Xarelto 1
- 50458-0579 Xarelto 1
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