"51128-501-02" National Drug Code (NDC)

Montelukast 90 TABLET, FILM COATED in 1 BOTTLE (51128-501-02)
(Recipharm Pharmaservices Private Limited)

NDC Code51128-501-02
Package Description90 TABLET, FILM COATED in 1 BOTTLE (51128-501-02)
Product NDC51128-501
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141201
Marketing Category NameANDA
Application NumberANDA202859
ManufacturerRecipharm Pharmaservices Private Limited
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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