"70518-3672-0" National Drug Code (NDC)

Methotrexate 30 TABLET in 1 BLISTER PACK (70518-3672-0)
(REMEDYREPACK INC.)

NDC Code70518-3672-0
Package Description30 TABLET in 1 BLISTER PACK (70518-3672-0)
Product NDC70518-3672
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230306
Marketing Category NameANDA
Application NumberANDA210454
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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