FDA NDC Directory · JSON-LD · Markdown

Zafirlukast

NDC 68084-059 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA090372
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZAFIRLUKAST (20 mg/1)
Marketing started20130603
Package count1

External sources

Source: openFDA. Public-domain (CC0).