Rheumatrex - 67253-580-47 - (Methotrexate)

Alphabetical Index


Drug Information of Rheumatrex

Product NDC: 67253-580
Proprietary Name: Rheumatrex
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 Rheumatrex

Product NDC: 67253-580
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA008085
Marketing Category: NDA
Start Marketing Date: 19530712

Package Information of Rheumatrex

Package NDC: 67253-580-47
Package Description: 4 BLISTER PACK in 1 CARTON (67253-580-47) > 7 TABLET in 1 BLISTER PACK

NDC Information of Rheumatrex

NDC Code 67253-580-47
Proprietary Name Rheumatrex
Package Description 4 BLISTER PACK in 1 CARTON (67253-580-47) > 7 TABLET in 1 BLISTER PACK
Product NDC 67253-580
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methotrexate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19530712
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 Rheumatrex


General Information