Drugplain

BENLYSTA 400 mg/5mL

belimumab · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · GlaxoSmithKline LLC

No Recall History
Plain English

BENLYSTA is a injection, powder, lyophilized, for solution containing belimumab at 400 mg/5mL, taken intravenous. Manufactured by GlaxoSmithKline LLC.

Key Facts

Brand Name
BENLYSTA
Generic Name
belimumab
NDC Code (Product)
49401-102
Manufacturer
GlaxoSmithKline LLC
Strength
400 mg/5mL
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
BLA125370
Drug Class
B Lymphocyte Stimulator-specific Inhibitor [EPC]
Marketing Start
03/10/2011

Recall History

No Recall History

Frequently Asked Questions

What is BENLYSTA used for?

BENLYSTA contains belimumab. It is a injection, powder, lyophilized, for solution taken intravenous. Consult your doctor for specific uses.

Is BENLYSTA a controlled substance?

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

What is the generic name for BENLYSTA?

The generic name for BENLYSTA is belimumab. There are no other listed brand versions of belimumab.

What is the NDC code for BENLYSTA 400 mg/5mL?

The NDC (National Drug Code) for BENLYSTA 400 mg/5mL is 49401-102, listed by GlaxoSmithKline LLC.

Product NDC

49401-102

Package NDC

49401-102-01

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

Data from openFDA · Public domain (CC0 1.0)