"67253-580-47" National Drug Code (NDC)

Rheumatrex 4 BLISTER PACK in 1 CARTON (67253-580-47) > 7 TABLET in 1 BLISTER PACK
(Par Pharmaceutical)

NDC Code67253-580-47
Package Description4 BLISTER PACK in 1 CARTON (67253-580-47) > 7 TABLET in 1 BLISTER PACK
Product NDC67253-580
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameRheumatrex
Proprietary Name SuffixDose Pack
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date19531207
Marketing Category NameNDA
Application NumberNDA008085
ManufacturerPar Pharmaceutical
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

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