Package 70518-4348-0

Brand: fluticasone propionate and salmeterol diskus

Generic: fluticasone propionate and salmeterol
NDC Package

Package Facts

Identity

Package NDC 70518-4348-0
Digits Only 7051843480
Product NDC 70518-4348
Description

1 INHALER in 1 CARTON (70518-4348-0) / 60 POWDER in 1 INHALER

Marketing

Marketing Status
Marketed Since 2025-07-10
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": "3ba0b267-1c17-6017-e063-6294a90ac389", "openfda": {"unii": ["O2GMZ0LF5W", "6EW8Q962A5"], "rxcui": ["896228"], "spl_set_id": ["197b7628-71aa-4fa2-94df-d617c0f2c986"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (70518-4348-0)  / 60 POWDER in 1 INHALER", "package_ndc": "70518-4348-0", "marketing_start_date": "20250710"}], "brand_name": "Fluticasone Propionate and Salmeterol DISKUS", "product_id": "70518-4348_3ba0b267-1c17-6017-e063-6294a90ac389", "dosage_form": "POWDER", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "70518-4348", "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": "500 ug/1"}, {"name": "SALMETEROL XINAFOATE", "strength": "50 ug/1"}], "application_number": "NDA021077", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250710", "listing_expiration_date": "20261231"}