"68071-1652-9" National Drug Code (NDC)

Montelukast 90 TABLET, FILM COATED in 1 BOTTLE (68071-1652-9)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-1652-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68071-1652-9)
Product NDC68071-1652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141201
Marketing Category NameANDA
Application NumberANDA202859
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

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