"68382-775-05" National Drug Code (NDC)

Methotrexate 500 TABLET in 1 BOTTLE (68382-775-05)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-775-05
Package Description500 TABLET in 1 BOTTLE (68382-775-05)
Product NDC68382-775
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20170209
Marketing Category NameANDA
Application NumberANDA207812
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameMETHOTREXATE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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