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"70518-3133-1" National Drug Code (NDC)

Montelukast 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3133-1)
(REMEDYREPACK INC.)

NDC Code70518-3133-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3133-1)
Product NDC70518-3133
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast
Non-Proprietary NameMontelukast
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210618
Marketing Category NameANDA
Application NumberANDA202843
ManufacturerREMEDYREPACK 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/70518-3133-1





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