Package 71205-262-60
Brand: fluticasone propionate and salmeterol diskus
Generic: fluticasone propionate and salmeterolPackage Facts
Identity
Package NDC
71205-262-60
Digits Only
7120526260
Product NDC
71205-262
Description
1 INHALER in 1 CARTON (71205-262-60) / 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": "632fef94-b34c-4c82-8b8a-8e573bad4dd5", "openfda": {"unii": ["O2GMZ0LF5W", "6EW8Q962A5"], "rxcui": ["896209"], "spl_set_id": ["6915bd5d-b792-4b1b-8221-7eeb0a8638ba"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (71205-262-60) / 60 POWDER in 1 INHALER", "package_ndc": "71205-262-60", "marketing_start_date": "20190501"}], "brand_name": "Fluticasone Propionate and Salmeterol DISKUS", "product_id": "71205-262_632fef94-b34c-4c82-8b8a-8e573bad4dd5", "dosage_form": "POWDER", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "71205-262", "generic_name": "fluticasone propionate and salmeterol", "labeler_name": "Proficient Rx LP", "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"}