Mycophenolate Mofetil 68071-3767
Product NDC
68071-3767- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 6, 2010
- Listing Expires
- December 31, 2026
- Application
- ANDA090456
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Mycophenolate Mofetil | 500 mg/1 |
Drug Class
Antimetabolite Immunosuppressant [EPC]
Packaging Options(1)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)