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"70771-1058-0" National Drug Code (NDC)

Methotrexate 1000 TABLET in 1 BOTTLE (70771-1058-0)
(Zydus Lifesciences Limited)

NDC Code70771-1058-0
Package Description1000 TABLET in 1 BOTTLE (70771-1058-0)
Product NDC70771-1058
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20170209
Marketing Category NameANDA
Application NumberANDA207812
ManufacturerZydus Lifesciences Limited
Substance NameMETHOTREXATE
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/70771-1058-0





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