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"70518-0172-1" National Drug Code (NDC)

Montelukast Sodium 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0172-1)
(REMEDYREPACK INC.)

NDC Code70518-0172-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0172-1)
Product NDC70518-0172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMontelukast Sodium
Non-Proprietary NameMontelukast Sodium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170123
Marketing Category NameANDA
Application NumberANDA202717
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/70518-0172-1





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