"52343-037-99" National Drug Code (NDC)

Montelukast Sodium 1000 TABLET, FILM COATED in 1 BOTTLE (52343-037-99)
(ACETRIS HEALTH, LLC)

NDC Code52343-037-99
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (52343-037-99)
Product NDC52343-037
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast Sodium
Non-Proprietary NameMontelukast Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120803
Marketing Category NameANDA
Application NumberANDA202468
ManufacturerACETRIS HEALTH, LLC
Substance NameMONTELUKAST SODIUM
Strength10
Strength Unitmg/1
Pharmacy ClassesLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]

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