Drug application
LORATADINE REDIDOSE (LORATADINE)
Drugs@FDA ANDA 077153 · SUN PHARM INDS LTD
Key facts
| Drug name | LORATADINE REDIDOSE |
|---|---|
| Active ingredients | LORATADINE |
| Application type | ANDA |
| Application number | 077153 |
| Company | SUN PHARM INDS LTD |
| Dosage forms | TABLET, ORALLY DISINTEGRATING, ORAL |
| Strength | 10MG |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Apr 11, 2007 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 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.