Drug application
PREDAMIDE (PREDNISOLONE ACETATE, SULFACETAMIDE SODIUM)
Drugs@FDA ANDA 088059 · EPIC PHARMA LLC
Key facts
| Drug name | PREDAMIDE |
|---|---|
| Active ingredients | PREDNISOLONE ACETATE, SULFACETAMIDE SODIUM |
| Application type | ANDA |
| Application number | 088059 |
| Company | EPIC PHARMA LLC |
| Dosage forms | SUSPENSION/DROPS, OPHTHALMIC |
| Strength | 0.5%;10% |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jul 29, 1983 |
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.