NDC Code | 63323-137-20 |
Package Description | 1 VIAL in 1 CARTON (63323-137-20) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
Product NDC | 63323-137 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bleomycin |
Non-Proprietary Name | Bleomycin Sulfate |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAPLEURAL; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20090213 |
Marketing Category Name | ANDA |
Application Number | ANDA065185 |
Manufacturer | Fresenius Kabi USA, LLC |
Substance Name | BLEOMYCIN SULFATE |
Strength | 30 |
Strength Unit | [USP'U]/1 |
Pharmacy Classes | Cytoprotective Agent [EPC] |