Drug application
MYHIBBIN (MYCOPHENOLATE MOFETIL)
Drugs@FDA NDA 216482 · AZURITY
Key facts
| Drug name | MYHIBBIN |
|---|---|
| Active ingredients | MYCOPHENOLATE MOFETIL |
| Application type | NDA |
| Application number | 216482 |
| Company | AZURITY |
| Dosage forms | SUSPENSION, ORAL |
| Strength | 200MG/ML |
| Marketing status | Prescription |
| Reference listed drug | Yes |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | May 1, 2024 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- Yes FDA reviews on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: