Class III ยท Low risk
Bleomycin for Injection
Labeling: Not elsewhere classified: Mislabeling
National Drug Code
Is NDC 0143-9240-01 recalled?
Bleomycin · 1 VIAL in 1 BOX, UNIT-DOSE (0143-9240-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL
Yes — this exact package was recalled
1 FDA recall names the code 0143-9240-01 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
- Bleomycin
- Strength
- BLEOMYCIN SULFATE 15 [USP'U]/1
- Form
- Injection, Powder, Lyophilized, for Solution · Intramuscular, Intrapleural, Intravenous, Subcutaneous
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 0143-9240
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
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