advair hfa
Generic: fluticasone propionate and salmeterol xinafoate
Labeler: glaxosmithkline llcDrug Facts
Product Profile
Brand Name
advair hfa
Generic Name
fluticasone propionate and salmeterol xinafoate
Labeler
glaxosmithkline llc
Dosage Form
AEROSOL, METERED
Routes
Active Ingredients
fluticasone propionate 230 ug/1, salmeterol xinafoate 21 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
0173-0717
Product ID
0173-0717_5107b97c-28b3-42a4-8da2-54b5dc05778e
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA021254
Listing Expiration
2027-12-31
Marketing Start
2009-03-06
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01730717
Hyphenated Format
0173-0717
Supplemental Identifiers
RxCUI
UNII
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
advair hfa (source: ndc)
Generic Name
fluticasone propionate and salmeterol xinafoate (source: ndc)
Application Number
NDA021254 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 230 ug/1
- 21 ug/1
Packaging
- 1 INHALER in 1 CARTON (0173-0717-20) / 120 AEROSOL, METERED in 1 INHALER
- 1 INHALER in 1 CARTON (0173-0717-22) / 60 AEROSOL, METERED in 1 INHALER
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "5107b97c-28b3-42a4-8da2-54b5dc05778e", "openfda": {"unii": ["6EW8Q962A5", "O2GMZ0LF5W"], "rxcui": ["896231", "896235", "896236", "896237", "896239", "896243", "896244", "896245", "896267", "896271", "896272", "896273"], "spl_set_id": ["dfaca6f9-3277-47b2-319d-1377917cb54c"], "manufacturer_name": ["GlaxoSmithKline LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (0173-0717-20) / 120 AEROSOL, METERED in 1 INHALER", "package_ndc": "0173-0717-20", "marketing_start_date": "20090306"}, {"sample": false, "description": "1 INHALER in 1 CARTON (0173-0717-22) / 60 AEROSOL, METERED in 1 INHALER", "package_ndc": "0173-0717-22", "marketing_start_date": "20090306"}], "brand_name": "ADVAIR HFA", "product_id": "0173-0717_5107b97c-28b3-42a4-8da2-54b5dc05778e", "dosage_form": "AEROSOL, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "0173-0717", "generic_name": "fluticasone propionate and salmeterol xinafoate", "labeler_name": "GlaxoSmithKline LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ADVAIR HFA", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "230 ug/1"}, {"name": "SALMETEROL XINAFOATE", "strength": "21 ug/1"}], "application_number": "NDA021254", "marketing_category": "NDA", "marketing_start_date": "20090306", "listing_expiration_date": "20271231"}