Drug application
CALDOLOR (IBUPROFEN)
Drugs@FDA NDA 022348 · APOTEX
Key facts
| Drug name | CALDOLOR |
|---|---|
| Active ingredients | IBUPROFEN |
| Application type | NDA |
| Application number | 022348 |
| Company | APOTEX |
| Dosage forms | SOLUTION, INTRAVENOUS |
| Strength | 400MG/4ML (100MG/ML) |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | Jun 11, 2009 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 10–99 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: