Package 50090-4213-0

{"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"}