"33342-102-39" National Drug Code (NDC)

Montelukast 90 TABLET in 1 BLISTER PACK (33342-102-39)
(Macleods Pharmaceuticals Limited)

NDC Code33342-102-39
Package Description90 TABLET in 1 BLISTER PACK (33342-102-39)
Product NDC33342-102
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET
UsageORAL
Start Marketing Date20140911
Marketing Category NameANDA
Application NumberANDA203366
ManufacturerMacleods Pharmaceuticals Limited
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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