Home
>
National Drug Code (NDC)
>
METHOTREXATE SODIUM
METHOTREXATE SODIUM - 75840-111-00 - (METHOTREXATE SODIUM)
Drug Information of METHOTREXATE SODIUM
| Product NDC: | 75840-111 |
| Proprietary Name: | METHOTREXATE SODIUM |
| Non Proprietary Name: | METHOTREXATE SODIUM |
| Active Ingredient(s): | 2.5 mg/1 & nbsp; METHOTREXATE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of METHOTREXATE SODIUM
| Product NDC: | 75840-111 |
| Labeler Name: | GenPak Solutions LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA008085 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20121001 |
Package Information of METHOTREXATE SODIUM
| Package NDC: | 75840-111-00 |
| Package Description: | 10 BOX in 1 BLISTER PACK (75840-111-00) > 100 TABLET in 1 BOX (75840-111-01) |
NDC Information of METHOTREXATE SODIUM
| NDC Code | 75840-111-00 |
| Proprietary Name | METHOTREXATE SODIUM |
| Package Description | 10 BOX in 1 BLISTER PACK (75840-111-00) > 100 TABLET in 1 BOX (75840-111-01) |
| Product NDC | 75840-111 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | METHOTREXATE SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20121001 |
| Marketing Category Name | NDA |
| Labeler Name | GenPak Solutions LLC |
| Substance Name | METHOTREXATE SODIUM |
| Strength Number | 2.5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA] |
