Drug application
SULSTER (PREDNISOLONE SODIUM PHOSPHATE, SULFACETAMIDE SODIUM)
Drugs@FDA ANDA 074511 · EPIC PHARMA LLC
Key facts
| Drug name | SULSTER |
|---|---|
| Active ingredients | PREDNISOLONE SODIUM PHOSPHATE, SULFACETAMIDE SODIUM |
| Application type | ANDA |
| Application number | 074511 |
| Company | EPIC PHARMA LLC |
| Dosage forms | SOLUTION/DROPS, OPHTHALMIC |
| Strength | EQ 0.23% PHOSPHATE;10% |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jul 30, 1996 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- No FDA letters on file
- Yes FDA reviews on file
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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: