| NDC Code | 51144-050-01 | 
|---|
			| Package Description | 1 VIAL, SINGLE-DOSE in 1 BOX (51144-050-01)  / 10.5 mL in 1 VIAL, SINGLE-DOSE | 
|---|
			| Product NDC | 51144-050 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Adcetris | 
|---|
			
			| Non-Proprietary Name | Brentuximab Vedotin | 
|---|
			| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION | 
|---|
			| Usage | INTRAVENOUS | 
|---|
			| Start Marketing Date | 20110825 | 
|---|
			
			| Marketing Category Name | BLA | 
|---|
			| Application Number | BLA125388 | 
|---|
			| Manufacturer | SEAGEN INC. | 
|---|
			| Substance Name | BRENTUXIMAB VEDOTIN | 
|---|
			| Strength | 50 | 
|---|
			| Strength Unit | mg/10.5mL | 
|---|
			| Pharmacy Classes | CD30-directed Antibody Interactions [MoA], CD30-directed Immunoconjugate [EPC], Immunoconjugates [CS], Microtubule Inhibition [PE] | 
|---|