"72865-175-10" National Drug Code (NDC)

Montelukast 1000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)
(XLCare Pharmaceuticals Inc.)

NDC Code72865-175-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)
Product NDC72865-175
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210211
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerXLCare Pharmaceuticals Inc.
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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