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"61786-417-03" National Drug Code (NDC)

Methotrexate 20 TABLET in 1 BOTTLE (61786-417-03)
(REMEDYREPACK INC.)

NDC Code61786-417-03
Package Description20 TABLET in 1 BOTTLE (61786-417-03)
Product NDC61786-417
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20160311
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/61786-417-03





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