VASOCIDIN (PREDNISOLONE SODIUM PHOSPHATE; SULFACETA) — FDA Approval NDA018988 (NOVARTIS)
VASOCIDIN (PREDNISOLONE SODIUM PHOSPHATE; SULFACETA) — FDA Approval NDA018988 (NOVARTIS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: VASOCIDIN; Active ingredients: PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM; Application number: NDA018988.
| Brand name | VASOCIDIN |
|---|---|
| Active ingredients | PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM |
| Application number | NDA018988 |
| Sponsor | NOVARTIS |
| Dosage form | SOLUTION/DROPS |
| Route | OPHTHALMIC |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19880826 |
| Source | openFDA Drugs@FDA |
$1499/mo
Try DrugApprovals →