Methotrexate 00904-7141
Product NDC
00904-7141- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 9, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207812
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methotrexate | 2.5 mg/1 |
Drug Class
Folate Analog Metabolic Inhibitor [EPC]Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]
Packaging Options(1)
20 BLISTER PACK in 1 CARTON (0904-7141-10) / 1 TABLET in 1 BLISTER PACK