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"47335-235-83" National Drug Code (NDC)

Methotrexate 100 TABLET in 1 BOTTLE (47335-235-83)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-235-83
Package Description100 TABLET in 1 BOTTLE (47335-235-83)
Product NDC47335-235
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate Sodium
Dosage FormTABLET
UsageORAL
Start Marketing Date20171110
Marketing Category NameANDA
Application NumberANDA201749
ManufacturerSun Pharmaceutical Industries, Inc.
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/47335-235-83





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