Drug application
CHILDREN'S CETIRIZINE HYDROCHLORIDE ALLERGY (CETIRIZINE HYDROCHLORIDE)
Drugs@FDA ANDA 090142 · SUN PHARM
Key facts
| Drug name | CHILDREN'S CETIRIZINE HYDROCHLORIDE ALLERGY |
|---|---|
| Active ingredients | CETIRIZINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 090142 |
| Company | SUN PHARM |
| Dosage forms | TABLET, CHEWABLE, ORAL |
| Strength | 5MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Aug 30, 2011 |
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.