Strength
500; 50 ug/1; ug/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093751631
Classification
Generic
Dosage Form
POWDER
Route
RESPIRATORY (INHALATION)
Last Updated
4/22/2026
Active Ingredients
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATEApproval Type
Generic (ANDA)
FDA Application
ANDA213948On Market Since
3/23/2022
Pharmacological Classes
Adrenergic beta2-Agonists
Corticosteroid Hormone Receptor Agonists
Corticosteroid
beta2-Adrenergic Agonist
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