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"71335-1979-3" National Drug Code (NDC)

Montelukast 7 TABLET, FILM COATED in 1 BOTTLE (71335-1979-3)
(Bryant Ranch Prepack)

NDC Code71335-1979-3
Package Description7 TABLET, FILM COATED in 1 BOTTLE (71335-1979-3)
Product NDC71335-1979
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140910
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerBryant Ranch Prepack
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-1979-3





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