nucala
Generic: mepolizumab
Labeler: glaxosmithkline llcDrug Facts
Product Profile
Brand Name
nucala
Generic Name
mepolizumab
Labeler
glaxosmithkline llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
mepolizumab 40 mg/.4mL
Manufacturer
Identifiers & Regulatory
Product NDC
0173-0904
Product ID
0173-0904_869b75ba-b2a0-406e-9ed2-136b75763d78
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA761122
Listing Expiration
2026-12-31
Marketing Start
2022-01-22
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01730904
Hyphenated Format
0173-0904
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
nucala (source: ndc)
Generic Name
mepolizumab (source: ndc)
Application Number
BLA761122 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/.4mL
Packaging
- 1 SYRINGE in 1 CARTON (0173-0904-42) / .4 mL in 1 SYRINGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "869b75ba-b2a0-406e-9ed2-136b75763d78", "openfda": {"nui": ["N0000191872", "N0000191871"], "unii": ["90Z2UF0E52"], "rxcui": ["1720601", "1720606", "2170990", "2170993", "2173820", "2173822", "2596444", "2596445"], "spl_set_id": ["fefb887c-e4ac-431e-8893-e9d1a5a63fea"], "pharm_class_epc": ["Interleukin-5 Antagonist [EPC]"], "pharm_class_moa": ["Interleukin-5 Antagonists [MoA]"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE in 1 CARTON (0173-0904-42) / .4 mL in 1 SYRINGE", "package_ndc": "0173-0904-42", "marketing_start_date": "20220122"}], "brand_name": "Nucala", "product_id": "0173-0904_869b75ba-b2a0-406e-9ed2-136b75763d78", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Interleukin-5 Antagonist [EPC]", "Interleukin-5 Antagonists [MoA]"], "product_ndc": "0173-0904", "generic_name": "mepolizumab", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nucala", "active_ingredients": [{"name": "MEPOLIZUMAB", "strength": "40 mg/.4mL"}], "application_number": "BLA761122", "marketing_category": "BLA", "marketing_start_date": "20220122", "listing_expiration_date": "20261231"}