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Fluticasone Propionate

NDC 49035-362 · HUMAN OTC DRUG · SPRAY, METERED

Labeler / ManufacturerWalmart
Marketing categoryAbbreviated NDA (generic) · App ANDA208150
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsFLUTICASONE PROPIONATE (50 ug/1)
Marketing started20171023
Marketing ended20261031
Package count1

External sources

Source: openFDA. Public-domain (CC0).