Trexall - 51285-368-01 - (methotrexate)

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Drug Information of Trexall

Product NDC: 51285-368
Proprietary Name: Trexall
Non Proprietary Name: methotrexate
Active Ingredient(s): 10    mg/1 & nbsp;   methotrexate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Trexall

Product NDC: 51285-368
Labeler Name: Teva Women's Health, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040385
Marketing Category: ANDA
Start Marketing Date: 20010503

Package Information of Trexall

Package NDC: 51285-368-01
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (51285-368-01)

NDC Information of Trexall

NDC Code 51285-368-01
Proprietary Name Trexall
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (51285-368-01)
Product NDC 51285-368
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name methotrexate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20010503
Marketing Category Name ANDA
Labeler Name Teva Women's Health, Inc.
Substance Name METHOTREXATE SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA]

Complete Information of Trexall


General Information