NDC 0173-0881

Nucala 100 mg per 1 mL injection, powder, for 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.

Product details

Generic drug
Mepolizumab: every company that makes it
Form
injection, powder, for solution, subcutaneous
Strength
100 mg per 1 mL
Approval
BLA BLA125526
On the market since
Nov 4, 2015
Package NDCs
0173-0881-01 0173-0881-61
Official label
DailyMed (National Library of Medicine), updated Aug 6, 2025

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