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Methotrexate Sodium - 63629-1472-4 - (Methotrexate Sodium)

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Drug Information of Methotrexate Sodium

Product NDC: 63629-1472
Proprietary Name: Methotrexate Sodium
Non Proprietary Name: Methotrexate Sodium
Active Ingredient(s): 2.5    mg/1 & nbsp;   Methotrexate Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methotrexate Sodium

Product NDC: 63629-1472
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040054
Marketing Category: ANDA
Start Marketing Date: 19940801

Package Information of Methotrexate Sodium

Package NDC: 63629-1472-4
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (63629-1472-4)

NDC Information of Methotrexate Sodium

NDC Code 63629-1472-4
Proprietary Name Methotrexate Sodium
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (63629-1472-4)
Product NDC 63629-1472
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methotrexate Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19940801
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name METHOTREXATE SODIUM
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Complete Information of Methotrexate Sodium


General Information