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"70518-0223-1" National Drug Code (NDC)

Methotrexate 20 TABLET in 1 BOTTLE, PLASTIC (70518-0223-1)
(REMEDYREPACK INC.)

NDC Code70518-0223-1
Package Description20 TABLET in 1 BOTTLE, PLASTIC (70518-0223-1)
Product NDC70518-0223
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20170215
Marketing Category NameNDA
Application NumberNDA008085
ManufacturerREMEDYREPACK INC.
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0223-1





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