"61786-417-02" National Drug Code (NDC)

Methotrexate 30 TABLET in 1 BLISTER PACK (61786-417-02)
(REMEDYREPACK INC.)

NDC Code61786-417-02
Package Description30 TABLET in 1 BLISTER PACK (61786-417-02)
Product NDC61786-417
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20150923
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]

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