Drug application
DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE (DORZOLAMIDE HYDROCHLORIDE, TIMOLOL MALEATE)
Drugs@FDA ANDA 091180 · ZAMBON SPA
Key facts
| Drug name | DORZOLAMIDE HYDROCHLORIDE AND TIMOLOL MALEATE |
|---|---|
| Active ingredients | DORZOLAMIDE HYDROCHLORIDE, TIMOLOL MALEATE |
| Application type | ANDA |
| Application number | 091180 |
| Company | ZAMBON SPA |
| Dosage forms | SOLUTION/DROPS, OPHTHALMIC |
| Strength | EQ 2% BASE;EQ 0.5% BASE |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Dec 4, 2013 |
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.