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"67253-320-10" National Drug Code (NDC)

Methotrexate 100 TABLET in 1 BOTTLE (67253-320-10)
(Par Pharmaceutical, Inc.)

NDC Code67253-320-10
Package Description100 TABLET in 1 BOTTLE (67253-320-10)
Product NDC67253-320
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date19531207
End Marketing Date20210228
Marketing Category NameNDA
Application NumberNDA008085
ManufacturerPar Pharmaceutical, Inc.
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67253-320-10





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