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Methotrexate Sodium - 54868-3826-0 - (methotrexate sodium)

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Drug Information of Methotrexate Sodium

Product NDC: 54868-3826
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: 54868-3826
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081099
Marketing Category: ANDA
Start Marketing Date: 20071205

Package Information of Methotrexate Sodium

Package NDC: 54868-3826-0
Package Description: 16 TABLET in 1 BOTTLE, PLASTIC (54868-3826-0)

NDC Information of Methotrexate Sodium

NDC Code 54868-3826-0
Proprietary Name Methotrexate Sodium
Package Description 16 TABLET in 1 BOTTLE, PLASTIC (54868-3826-0)
Product NDC 54868-3826
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methotrexate sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071205
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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