Mycophenolate mofetil
- Product NDC
- 68071-3767
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mycophenolate mofetil
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA090456
- Marketing category
- ANDA
- Substance
- MYCOPHENOLATE MOFETIL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3767-6 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6) | 2025-01-13 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Mycophenolate mofetil | NuCare Pharmaceuticals, Inc. | 2025-01-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |