"68071-3991-9" National Drug Code (NDC)

Methotrexate 90 TABLET in 1 BOTTLE (68071-3991-9)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-3991-9
Package Description90 TABLET in 1 BOTTLE (68071-3991-9)
Product NDC68071-3991
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200824
Marketing Category NameANDA
Application NumberANDA213343
ManufacturerNuCare Pharmaceuticals, Inc.
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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