"70518-2603-2" National Drug Code (NDC)

Montelukast 30 TABLET in 1 BOTTLE, PLASTIC (70518-2603-2)
(REMEDYREPACK INC.)

NDC Code70518-2603-2
Package Description30 TABLET in 1 BOTTLE, PLASTIC (70518-2603-2)
Product NDC70518-2603
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET
UsageORAL
Start Marketing Date20200227
Marketing Category NameANDA
Application NumberANDA203366
ManufacturerREMEDYREPACK INC.
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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