Package 71205-262-60

Brand: fluticasone propionate and salmeterol diskus

Generic: fluticasone propionate and salmeterol
NDC Package

Package 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
Marketed Since 2019-05-01
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"}