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Fluticasone Propionate

NDC 70518-0880 · HUMAN PRESCRIPTION DRUG · SPRAY, METERED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA076504
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsFLUTICASONE PROPIONATE (50 ug/1)
Marketing started20180315
Package count1

External sources

Source: openFDA. Public-domain (CC0).