"48433-065-05" National Drug Code (NDC)

Methotrexate 20 BLISTER PACK in 1 CARTON (48433-065-05) / 1 TABLET in 1 BLISTER PACK (48433-065-01)
(Safecor Health LLC)

NDC Code48433-065-05
Package Description20 BLISTER PACK in 1 CARTON (48433-065-05) / 1 TABLET in 1 BLISTER PACK (48433-065-01)
Product NDC48433-065
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20260119
Marketing Category NameANDA
Application NumberANDA081235
ManufacturerSafecor Health LLC
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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