FDA NDC Directory · JSON-LD · Markdown

roflumilast

NDC 64380-786 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameROFLUMILAST
Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208247
Dosage form / routeTABLET · ORAL
Active ingredientsROFLUMILAST (500 ug/1)
Marketing started20221013
Package count2

External sources

Source: openFDA. Public-domain (CC0).