"70518-3133-0" National Drug Code (NDC)

Montelukast 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-0)
(REMEDYREPACK INC.)

NDC Code70518-3133-0
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-0)
Product NDC70518-3133
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210618
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerREMEDYREPACK INC.
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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