FDA NDC Directory · JSON-LD · Markdown

montelukast sodium

NDC 29300-220 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerUnichem Pharmaceuticals (USA), Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204290
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMONTELUKAST SODIUM (10 mg/1)
Marketing started20160101
Package count4

External sources

Source: openFDA. Public-domain (CC0).