Drug application
IBUPROFEN (IBUPROFEN)
Drugs@FDA ANDA 217261 · SUN PHARMA CANADA
Key facts
| Drug name | IBUPROFEN |
|---|---|
| Active ingredients | IBUPROFEN |
| Application type | ANDA |
| Application number | 217261 |
| Company | SUN PHARMA CANADA |
| Dosage forms | SUSPENSION/DROPS, ORAL |
| Strength | 40MG/ML |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Aug 8, 2023 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None 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.