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Methotrexate Sodium - 0054-4550-15 - (Methotrexate Sodium)

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Drug Information of Methotrexate Sodium

Product NDC: 0054-4550
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: 0054-4550
Labeler Name: Roxane Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040054
Marketing Category: ANDA
Start Marketing Date: 19940801

Package Information of Methotrexate Sodium

Package NDC: 0054-4550-15
Package Description: 36 TABLET in 1 BOTTLE, PLASTIC (0054-4550-15)

NDC Information of Methotrexate Sodium

NDC Code 0054-4550-15
Proprietary Name Methotrexate Sodium
Package Description 36 TABLET in 1 BOTTLE, PLASTIC (0054-4550-15)
Product NDC 0054-4550
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 Roxane Laboratories, Inc
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


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