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Rheumatrex
Rheumatrex - 67253-580-42 - (Methotrexate)
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: | 67253-580-42 |
| Package Description: | 4 BLISTER PACK in 1 CARTON (67253-580-42) > 2 TABLET in 1 BLISTER PACK |
NDC Information of Rheumatrex
| NDC Code | 67253-580-42 |
| Proprietary Name | Rheumatrex |
| Package Description | 4 BLISTER PACK in 1 CARTON (67253-580-42) > 2 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] |
