NDC 49401-088

Benlysta 200 mg per 1 mL solution

On the label: GlaxoSmithKline LLC.

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants GlaxoSmithKline LLC names for other drugs.

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Belimumab: every company that makes it
Form
solution, subcutaneous
Strength
200 mg per 1 mL
Approval
BLA BLA761043
On the market since
Jul 20, 2017
Package NDCs
49401-088-01 49401-088-02 49401-088-35 49401-088-42 49401-088-47 49401-088-50 49401-088-61
Official label
DailyMed (National Library of Medicine), updated Aug 21, 2026

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