FDA NDC Directory · JSON-LD · Markdown

Montelukast

NDC 68071-3855 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203366
Dosage form / routeTABLET · ORAL
Active ingredientsMONTELUKAST SODIUM (10 mg/1)
Marketing started20140911
Package count1

External sources

Source: openFDA. Public-domain (CC0).