"42708-042-30" National Drug Code (NDC)

Montelukast Sodium 30 TABLET, FILM COATED in 1 BOTTLE (42708-042-30)
(QPharma Inc)

NDC Code42708-042-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (42708-042-30)
Product NDC42708-042
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast Sodium
Non-Proprietary NameMontelukast Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120803
Marketing Category NameANDA
Application NumberANDA078605
ManufacturerQPharma Inc
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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