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"0904-7141-10" National Drug Code (NDC)

Methotrexate 20 BLISTER PACK in 1 CARTON (0904-7141-10) / 1 TABLET in 1 BLISTER PACK
(Major Pharmaceuticals)

NDC Code0904-7141-10
Package Description20 BLISTER PACK in 1 CARTON (0904-7141-10) / 1 TABLET in 1 BLISTER PACK
Product NDC0904-7141
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMethotrexate
Non-Proprietary NameMethotrexate
Dosage FormTABLET
UsageORAL
Start Marketing Date20170209
Marketing Category NameANDA
Application NumberANDA207812
ManufacturerMajor Pharmaceuticals
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/0904-7141-10





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