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"71335-2221-7" National Drug Code (NDC)

Methotrexate 90 TABLET in 1 BOTTLE (71335-2221-7)
(Bryant Ranch Prepack)

NDC Code71335-2221-7
Package Description90 TABLET in 1 BOTTLE (71335-2221-7)
Product NDC71335-2221
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200130
Marketing Category NameANDA
Application NumberANDA210454
ManufacturerBryant Ranch Prepack
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/71335-2221-7





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