Mycophenolate Mofetil 00781-5175
Product NDC
00781-5175- Manufacturer
- Sandoz Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 15, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA065451
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Mycophenolate Mofetil | 500 mg/1 |
Drug Class
Antimetabolite Immunosuppressant [EPC]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (0781-5175-01)
500 TABLET, FILM COATED in 1 BOTTLE (0781-5175-05)
1000 TABLET, FILM COATED in 1 BOTTLE (0781-5175-10)