| NDC Code | 0703-3155-01 | 
|---|
			| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3155-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | 
|---|
			| Product NDC | 0703-3155 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Bleomycin | 
|---|
			
			| Non-Proprietary Name | Bleomycin | 
|---|
			| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 
|---|
			| Usage | INTRAMUSCULAR; INTRAPLEURAL; INTRAVENOUS; SUBCUTANEOUS | 
|---|
			| Start Marketing Date | 20000630 | 
|---|
			| End Marketing Date | 20230831 | 
|---|
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA065033 | 
|---|
			| Manufacturer | Teva Parenteral Medicines, Inc. | 
|---|
			| Substance Name | BLEOMYCIN SULFATE | 
|---|
			| Strength | 30 | 
|---|
			| Strength Unit | [USP'U]/1 | 
|---|
			| Pharmacy Classes | Cytoprotective Agent [EPC] | 
|---|