Package 70518-4347-0

Brand: fluticasone propionate and salmeterol diskus

Generic: fluticasone propionate and salmeterol
NDC Package

Package Facts

Identity

Package NDC 70518-4347-0
Digits Only 7051843470
Product NDC 70518-4347
Description

1 INHALER in 1 CARTON (70518-4347-0) / 60 POWDER in 1 INHALER

Marketing

Marketing Status
Marketed Since 2025-05-29
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": "3ba1895a-2996-f42b-e063-6394a90a842b", "openfda": {"unii": ["O2GMZ0LF5W", "6EW8Q962A5"], "rxcui": ["896209"], "spl_set_id": ["1ce604aa-2535-4a3c-a64d-092f5d4f8194"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (70518-4347-0)  / 60 POWDER in 1 INHALER", "package_ndc": "70518-4347-0", "marketing_start_date": "20250529"}], "brand_name": "Fluticasone Propionate and Salmeterol DISKUS", "product_id": "70518-4347_3ba1895a-2996-f42b-e063-6394a90a842b", "dosage_form": "POWDER", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-4347", "generic_name": "fluticasone propionate and salmeterol", "labeler_name": "REMEDYREPACK INC.", "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": "20250529", "listing_expiration_date": "20261231"}