Drugplain

ADCETRIS 50 mg/10.5mL

brentuximab vedotin · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · SEAGEN INC.

No Recall History
Plain English

ADCETRIS is a injection, powder, lyophilized, for solution containing brentuximab vedotin at 50 mg/10.5mL, taken intravenous. Manufactured by SEAGEN INC..

Key Facts

Brand Name
ADCETRIS
Generic Name
brentuximab vedotin
NDC Code (Product)
51144-050
Manufacturer
SEAGEN INC.
Strength
50 mg/10.5mL
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
BLA125388
Drug Class
CD30-directed Immunoconjugate [EPC]
Marketing Start
08/25/2011

Recall History

No Recall History

Frequently Asked Questions

What is ADCETRIS used for?

ADCETRIS contains brentuximab vedotin. It is a injection, powder, lyophilized, for solution taken intravenous. Consult your doctor for specific uses.

Is ADCETRIS a controlled substance?

ADCETRIS is not classified as a controlled substance by the DEA.

What is the generic name for ADCETRIS?

The generic name for ADCETRIS is brentuximab vedotin. There are no other listed brand versions of brentuximab vedotin.

What is the NDC code for ADCETRIS 50 mg/10.5mL?

The NDC (National Drug Code) for ADCETRIS 50 mg/10.5mL is 51144-050, listed by SEAGEN INC..

Product NDC

51144-050

Package NDC

51144-050-01

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)