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Fluticasone Propionate and Salmeterol

NDC 0527-6010 · HUMAN PRESCRIPTION DRUG · POWDER

Generic namefluticasone propionate and salmeterol
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214464
Dosage form / routePOWDER · RESPIRATORY (INHALATION)
Active ingredientsFLUTICASONE PROPIONATE (100 ug/1)
SALMETEROL XINAFOATE (50 ug/1)
Marketing started20260112
Package count1

External sources

Source: openFDA. Public-domain (CC0).