NDC 31722-879 – Mycophenolate Mofetil
Mycophenolate Mofetil 500 mg/1 · Tablet, Film Coated · Oral
Product NDC31722-879
Product details
- Brand name
- Mycophenolate Mofetil
- Generic name
- Mycophenolate Mofetil
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA208119
- Marketed since
- October 22, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Antimetabolite Immunosuppressant
Active ingredients
- Mycophenolate Mofetil 500 mg/1
Uses, dosage, side effects and warnings for Mycophenolate Mofetil →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 31722-879-01 | 100 TABLET, FILM COATED in 1 BOTTLE (31722-879-01) | Oct 22, 2024 |
| 31722-879-05 | 500 TABLET, FILM COATED in 1 BOTTLE (31722-879-05) | Oct 22, 2024 |
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