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METHOTREXATE - 55289-924-30 - (METHOTREXATE)

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Drug Information of METHOTREXATE

Product NDC: 55289-924
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: 55289-924
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008085
Marketing Category: NDA
Start Marketing Date: 19531207

Package Information of METHOTREXATE

Package NDC: 55289-924-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (55289-924-30)

NDC Information of METHOTREXATE

NDC Code 55289-924-30
Proprietary Name METHOTREXATE
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (55289-924-30)
Product NDC 55289-924
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 PD-Rx 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