"71335-1599-3" National Drug Code (NDC)

Montelukast Sodium 7 TABLET, FILM COATED in 1 BOTTLE (71335-1599-3)
(Bryant Ranch Prepack)

NDC Code71335-1599-3
Package Description7 TABLET, FILM COATED in 1 BOTTLE (71335-1599-3)
Product NDC71335-1599
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast Sodium
Non-Proprietary NameMontelukast Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130411
Marketing Category NameANDA
Application NumberANDA202717
ManufacturerBryant Ranch Prepack
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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