Drug application
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE (IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE)
Drugs@FDA ANDA 209235 · AUROBINDO PHARMA
Key facts
| Drug name | IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE |
|---|---|
| Active ingredients | IBUPROFEN, PSEUDOEPHEDRINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 209235 |
| Company | AUROBINDO PHARMA |
| Dosage forms | CAPSULE, ORAL |
| Strength | EQ 200MG FREE ACID AND POTASSIUM SALT;30MG |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Dec 1, 2017 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- No 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: