Package 50090-1245-0

Brand: flovent diskus

Generic: fluticasone propionate
NDC Package

Package Facts

Identity

Package NDC 50090-1245-0
Digits Only 5009012450
Product NDC 50090-1245
Description

1 INHALER in 1 CARTON (50090-1245-0) / 60 POWDER, METERED in 1 INHALER

Marketing

Marketing Status
Marketed Since 2014-11-28
Brand flovent diskus
Generic fluticasone propionate
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "fb05bfe4-e8d9-4abb-afe1-d651eaa4eefd", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["896018", "896019"], "spl_set_id": ["038e6c40-9421-40ef-874b-8f4d7110a74a"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (50090-1245-0)  / 60 POWDER, METERED in 1 INHALER", "package_ndc": "50090-1245-0", "marketing_start_date": "20141128"}], "brand_name": "FLOVENT DISKUS", "product_id": "50090-1245_fb05bfe4-e8d9-4abb-afe1-d651eaa4eefd", "dosage_form": "POWDER, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-1245", "generic_name": "fluticasone propionate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLOVENT", "brand_name_suffix": "DISKUS", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/1"}], "application_number": "NDA020833", "marketing_category": "NDA", "marketing_start_date": "20070508", "listing_expiration_date": "20261231"}