"70518-1398-1" National Drug Code (NDC)

Methotrexate 20 TABLET in 1 BOTTLE, PLASTIC (70518-1398-1)
(REMEDYREPACK INC.)

NDC Code70518-1398-1
Package Description20 TABLET in 1 BOTTLE, PLASTIC (70518-1398-1)
Product NDC70518-1398
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180904
Marketing Category NameANDA
Application NumberANDA207812
ManufacturerREMEDYREPACK INC.
Substance NameMETHOTREXATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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