fluticasone propionate and salmeterol

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

fluticasone propionate 232 ug/1, salmeterol xinafoate 14 ug/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3387
Product ID 50090-3387_4bf35a9c-39b0-4293-a1ae-5a1d1bc97c48
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA208799
Listing Expiration 2026-12-31
Marketing Start 2017-04-28

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 500903387
Hyphenated Format 50090-3387

Supplemental Identifiers

RxCUI
1918194 1918203 1918209
UNII
6EW8Q962A5 O2GMZ0LF5W

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 (source: ndc)
Generic Name fluticasone propionate and salmeterol (source: ndc)
Application Number NDA208799 (source: ndc)
Routes
RESPIRATORY (INHALATION)
source: ndc

Resolved Composition

Strengths
  • 232 ug/1
  • 14 ug/1
source: ndc
Packaging
  • 1 POUCH in 1 CARTON (50090-3387-0) / 1 POWDER, METERED in 1 POUCH
source: ndc

Packages (1)

50090-3387-0 1 POUCH in 1 CARTON (50090-3387-0) / 1 POWDER, METERED in 1 POUCH

Ingredients (2)

fluticasone propionate (232 ug/1) salmeterol xinafoate (14 ug/1)

Linked Drug Pages (1)

Fluticasone Propionate and Salmeterol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "4bf35a9c-39b0-4293-a1ae-5a1d1bc97c48", "openfda": {"unii": ["6EW8Q962A5", "O2GMZ0LF5W"], "rxcui": ["1918194", "1918203", "1918209"], "spl_set_id": ["77269609-fb89-47c7-97cc-22e0183e91ae"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 POUCH in 1 CARTON (50090-3387-0)  / 1 POWDER, METERED in 1 POUCH", "package_ndc": "50090-3387-0", "marketing_start_date": "20180305"}], "brand_name": "Fluticasone Propionate and Salmeterol", "product_id": "50090-3387_4bf35a9c-39b0-4293-a1ae-5a1d1bc97c48", "dosage_form": "POWDER, METERED", "pharm_class": ["Adrenergic beta2-Agonists [MoA]", "Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]", "beta2-Adrenergic Agonist [EPC]"], "product_ndc": "50090-3387", "generic_name": "Fluticasone Propionate and Salmeterol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluticasone Propionate and Salmeterol", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "232 ug/1"}, {"name": "SALMETEROL XINAFOATE", "strength": "14 ug/1"}], "application_number": "NDA208799", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20170428", "listing_expiration_date": "20261231"}