Drug application
BUDESONIDE (BUDESONIDE)
Drugs@FDA ANDA 216667 · EUGIA PHARMA
Key facts
| Drug name | BUDESONIDE |
|---|---|
| Active ingredients | BUDESONIDE |
| Application type | ANDA |
| Application number | 216667 |
| Company | EUGIA PHARMA |
| Dosage forms | SUSPENSION, INHALATION |
| Strength | 0.5MG/2ML |
| Marketing status | Prescription |
| TE codes | AN |
| Reference listed drug | No |
| Latest submission status date | Nov 29, 2023 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
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.