FDA NDC Directory · JSON-LD · Markdown

Roflumilast

NDC 0904-7483 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA208256
Dosage form / routeTABLET · ORAL
Active ingredientsROFLUMILAST (500 ug/1)
Marketing started20240522
Package count2

External sources

Source: openFDA. Public-domain (CC0).