"71335-1772-2" National Drug Code (NDC)

Methotrexate 12 TABLET in 1 BOTTLE (71335-1772-2)
(Bryant Ranch Prepack)

NDC Code71335-1772-2
Package Description12 TABLET in 1 BOTTLE (71335-1772-2)
Product NDC71335-1772
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200824
Marketing Category NameANDA
Application NumberANDA213343
ManufacturerBryant Ranch Prepack
Substance NameMETHOTREXATE SODIUM
Strength2.5
Strength Unitmg/1
Pharmacy ClassesFolate Analog Metabolic Inhibitor [EPC], Folic Acid Metabolism Inhibitors [MoA]

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