"51079-223-20" National Drug Code (NDC)

Montelukast Sodium 100 BLISTER PACK in 1 CARTON (51079-223-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-223-01)
(Mylan Institutional Inc.)

NDC Code51079-223-20
Package Description100 BLISTER PACK in 1 CARTON (51079-223-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-223-01)
Product NDC51079-223
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast Sodium
Non-Proprietary NameMontelukast Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120828
End Marketing Date20190930
Marketing Category NameANDA
Application NumberANDA079103
ManufacturerMylan Institutional Inc.
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

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