Methotrexate 00555-0572
Product NDC
00555-0572- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 1, 1990
- Listing Expires
- December 31, 2027
- Application
- ANDA081099
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Methotrexate Sodium | 2.5 mg/1 |
Drug Class
Folate Analog Metabolic Inhibitor [EPC]Folic Acid Metabolism Inhibitors [MoA]
Packaging Options(2)
100 TABLET in 1 BOTTLE (0555-0572-02)
36 TABLET in 1 BOTTLE (0555-0572-35)