FDA NDC Directory · JSON-LD · Markdown

Montelukast

NDC 68788-8099 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202843
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMONTELUKAST SODIUM (10 mg/1)
Marketing started20211006
Package count3

External sources

Source: openFDA. Public-domain (CC0).