Package 50090-4213-0
Brand: fluticasone propionate and salmeterol diskus
Generic: fluticasone propionate and salmeterolPackage Facts
Identity
Package NDC
50090-4213-0
Digits Only
5009042130
Product NDC
50090-4213
Description
1 INHALER in 1 CARTON (50090-4213-0) / 60 POWDER in 1 INHALER
Marketing
Marketing Status
Brand
fluticasone propionate and salmeterol diskus
Generic
fluticasone propionate and salmeterol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "0bd79006-13e5-4b32-b23e-e787bc8e0b0d", "openfda": {"unii": ["O2GMZ0LF5W", "6EW8Q962A5"], "rxcui": ["896209"], "spl_set_id": ["9e237635-6975-4930-9ce1-051d9e3bf615"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (50090-4213-0) / 60 POWDER in 1 INHALER", "package_ndc": "50090-4213-0", "marketing_start_date": "20190325"}], "brand_name": "Fluticasone Propionate and Salmeterol DISKUS", "product_id": "50090-4213_0bd79006-13e5-4b32-b23e-e787bc8e0b0d", "dosage_form": "POWDER", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "50090-4213", "generic_name": "fluticasone propionate and salmeterol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluticasone Propionate and Salmeterol", "brand_name_suffix": "DISKUS", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "250 ug/1"}, {"name": "SALMETEROL XINAFOATE", "strength": "50 ug/1"}], "application_number": "NDA021077", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190208", "listing_expiration_date": "20261231"}