"0555-0572-35" National Drug Code (NDC)

Methotrexate 36 TABLET in 1 BOTTLE (0555-0572-35)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0555-0572-35
Package Description36 TABLET in 1 BOTTLE (0555-0572-35)
Product NDC0555-0572
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date19901101
Marketing Category NameANDA
Application NumberANDA081099
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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