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METHOTREXATE - 67253-320-10 - (METHOTREXATE)

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Drug Information of METHOTREXATE

Product NDC: 67253-320
Proprietary Name: METHOTREXATE
Non Proprietary Name: METHOTREXATE
Active Ingredient(s): 2.5    mg/1 & nbsp;   METHOTREXATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of METHOTREXATE

Product NDC: 67253-320
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008085
Marketing Category: NDA
Start Marketing Date: 19531207

Package Information of METHOTREXATE

Package NDC: 67253-320-10
Package Description: 100 TABLET in 1 BOTTLE (67253-320-10)

NDC Information of METHOTREXATE

NDC Code 67253-320-10
Proprietary Name METHOTREXATE
Package Description 100 TABLET in 1 BOTTLE (67253-320-10)
Product NDC 67253-320
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METHOTREXATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19531207
Marketing Category Name NDA
Labeler Name DAVA Pharmaceuticals, 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


General Information