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Montelukast Sodium

NDC 55111-725 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerDr.Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA201582
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMONTELUKAST SODIUM (10 mg/1)
Marketing started20120806
Package count5

External sources

Source: openFDA. Public-domain (CC0).