Methotrexate Sodium is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Methotrexate Sodium.
| Product ID | 70518-2711_a61925ad-a8c6-49cd-e053-2a95a90a301c |
| NDC | 70518-2711 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Methotrexate Sodium |
| Generic Name | Methotrexate Sodium |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2020-04-27 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA040054 |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | METHOTREXATE SODIUM |
| Active Ingredient Strength | 3 mg/1 |
| Pharm Classes | Folate Analog Metabolic Inhibitor [EPC],Folic Acid Metabolism Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2021-12-31 |
| Marketing Start Date | 2020-04-27 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA040054 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2020-04-27 |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0054-4550 | Methotrexate Sodium | Methotrexate Sodium |
| 0054-8550 | Methotrexate Sodium | Methotrexate Sodium |
| 63629-1472 | Methotrexate Sodium | Methotrexate Sodium |
| 66758-040 | Methotrexate Sodium | Methotrexate Sodium |
| 66758-041 | Methotrexate Sodium | Methotrexate Sodium |
| 70518-2711 | Methotrexate Sodium | Methotrexate Sodium |
| 75840-111 | METHOTREXATE SODIUM | METHOTREXATE SODIUM |
| 21695-111 | Methotrexate | Methotrexate sodium |
| 47335-235 | Methotrexate | Methotrexate Sodium |
| 50090-3418 | Methotrexate | Methotrexate Sodium |
| 63323-122 | Methotrexate | METHOTREXATE SODIUM |
| 63323-123 | Methotrexate | METHOTREXATE SODIUM |
| 70518-1251 | Methotrexate | Methotrexate Sodium |