Drug application
DORZOLAMIDE HYDROCHLORIDE (DORZOLAMIDE HYDROCHLORIDE)
Drugs@FDA ANDA 215004 · SOMERSET THERAPS LLC
Key facts
| Drug name | DORZOLAMIDE HYDROCHLORIDE |
|---|---|
| Active ingredients | DORZOLAMIDE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 215004 |
| Company | SOMERSET THERAPS LLC |
| Dosage forms | SOLUTION/DROPS, OPHTHALMIC |
| Strength | EQ 2% BASE |
| Marketing status | Prescription |
| TE codes | AT |
| Reference listed drug | No |
| Latest submission status date | Feb 11, 2025 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 10–99 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.