Package 50090-4214-0

{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "edadad9b-f6c8-42bb-b185-95743bb64e54", "openfda": {"unii": ["O2GMZ0LF5W", "6EW8Q962A5"], "rxcui": ["896228"], "spl_set_id": ["ccf98c0a-fc40-4e08-bdf2-145fe4537db5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (50090-4214-0)  / 60 POWDER in 1 INHALER", "package_ndc": "50090-4214-0", "marketing_start_date": "20190325"}], "brand_name": "Fluticasone Propionate and Salmeterol DISKUS", "product_id": "50090-4214_edadad9b-f6c8-42bb-b185-95743bb64e54", "dosage_form": "POWDER", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "50090-4214", "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": "500 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"}