"50090-6108-0" National Drug Code (NDC)

Montelukast 30 TABLET, FILM COATED in 1 BOTTLE (50090-6108-0)
(A-S Medication Solutions)

NDC Code50090-6108-0
Package Description30 TABLET, FILM COATED in 1 BOTTLE (50090-6108-0)
Product NDC50090-6108
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140910
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerA-S Medication Solutions
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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