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"69452-105-19" National Drug Code (NDC)

Montelukast 90 TABLET, FILM COATED in 1 BOTTLE (69452-105-19)
(Bionpharma Inc.)

NDC Code69452-105-19
Package Description90 TABLET, FILM COATED in 1 BOTTLE (69452-105-19)
Product NDC69452-105
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141201
End Marketing Date20211231
Marketing Category NameANDA
Application NumberANDA202859
ManufacturerBionpharma Inc.
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/69452-105-19





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