fluticasone propionate and salmeterol diskus

Generic: fluticasone propionate and salmeterol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name fluticasone propionate and salmeterol diskus
Generic Name fluticasone propionate and salmeterol
Labeler a-s medication solutions
Dosage Form POWDER
Routes
RESPIRATORY (INHALATION)
Active Ingredients

fluticasone propionate 250 ug/1, salmeterol xinafoate 50 ug/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-4213
Product ID 50090-4213_0bd79006-13e5-4b32-b23e-e787bc8e0b0d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA021077
Listing Expiration 2026-12-31
Marketing Start 2019-02-08

Pharmacologic Class

Classes
adrenergic beta2-agonists [moa] corticosteroid hormone receptor agonists [moa] corticosteroid [epc] beta2-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500904213
Hyphenated Format 50090-4213

Supplemental Identifiers

RxCUI
896209
UNII
O2GMZ0LF5W 6EW8Q962A5

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name fluticasone propionate and salmeterol diskus (source: ndc)
Generic Name fluticasone propionate and salmeterol (source: ndc)
Application Number NDA021077 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 250 ug/1
  • 50 ug/1
source: ndc
Packaging
  • 1 INHALER in 1 CARTON (50090-4213-0) / 60 POWDER in 1 INHALER
source: ndc

Packages (1)

50090-4213-0 1 INHALER in 1 CARTON (50090-4213-0) / 60 POWDER in 1 INHALER

Ingredients (2)

fluticasone propionate (250 ug/1) salmeterol xinafoate (50 ug/1)

Linked Drug Pages (1)

Fluticasone Propionate and Salmeterol DISKUS ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "0bd79006-13e5-4b32-b23e-e787bc8e0b0d", "openfda": {"unii": ["O2GMZ0LF5W", "6EW8Q962A5"], "rxcui": ["896209"], "spl_set_id": ["9e237635-6975-4930-9ce1-051d9e3bf615"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (50090-4213-0)  / 60 POWDER in 1 INHALER", "package_ndc": "50090-4213-0", "marketing_start_date": "20190325"}], "brand_name": "Fluticasone Propionate and Salmeterol DISKUS", "product_id": "50090-4213_0bd79006-13e5-4b32-b23e-e787bc8e0b0d", "dosage_form": "POWDER", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "50090-4213", "generic_name": "fluticasone propionate and salmeterol", "labeler_name": "A-S Medication Solutions", "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"}