"82982-040-30" National Drug Code (NDC)

Montelukast 30 TABLET, FILM COATED in 1 BOTTLE (82982-040-30)
(Pharmasource Meds, LLC)

NDC Code82982-040-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (82982-040-30)
Product NDC82982-040
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230329
End Marketing Date20241031
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerPharmasource Meds, LLC
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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