Class II · Moderate risk
Irinotecan Hydrochloride Injection
Superpotent Drug: High out of specification assay value results for potency.
National Drug Code
Is NDC 50742-0402-05 recalled?
Irinotecan Hydrochloride · 1 VIAL, GLASS in 1 CARTON (50742-402-05) / 5 mL in 1 VIAL, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 50742-0402-05 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
- Irinotecan Hydrochloride
- Strength
- IRINOTECAN HYDROCHLORIDE 100 mg/5mL
- Form
- Injection · Intravenous
- Labeler
- Ingenus Pharmaceuticals, LLC
- Type
- Human Prescription Drug
- Product code
- 50742-0402
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
- 50742-0208 See recall 1
- 50742-0304 See recall 1
- 50742-0308 See recall 1
- 50742-0317 Flunisolide 1
- 50742-0401 Irinotecan Hydrochloride 1
- 50742-0464 See recall 1
Free recall alerts
Know the day your medication is recalled
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