Strength
100; 50 ug/1; ug/1
Manufacturer
GlaxoSmithKline LLCNDC
00173069504
Classification
Brand
Dosage Form
POWDER
Route
RESPIRATORY (INHALATION)
Last Updated
1/1/2018
Active Ingredients
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATEApproval Type
New Drug (NDA)
FDA Application
NDA021077On Market Since
2/28/2001
Pharmacological Classes
Adrenergic beta2-Agonists
Corticosteroid Hormone Receptor Agonists
Corticosteroid
beta2-Adrenergic Agonist
FLUTICASONE-SALMETEROL 100-50
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FLUTICASONE-SALMETEROL 100-50
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