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