Drug application
CYCLOPENTOLATE HYDROCHLORIDE (CYCLOPENTOLATE HYDROCHLORIDE)
Drugs@FDA ANDA 205937 · SCIEGEN PHARMS
Key facts
| Drug name | CYCLOPENTOLATE HYDROCHLORIDE |
|---|---|
| Active ingredients | CYCLOPENTOLATE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 205937 |
| Company | SCIEGEN PHARMS |
| Dosage forms | SOLUTION/DROPS, OPHTHALMIC |
| Strength | 0.5% |
| Marketing status | Discontinued |
| TE codes | AT |
| Reference listed drug | No |
| Latest submission status date | Dec 9, 2015 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 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.