DEXACORT (DEXAMETHASONE SODIUM PHOSPHATE) — FDA Approval NDA014242 (UCB INC)
DEXACORT (DEXAMETHASONE SODIUM PHOSPHATE) — FDA Approval NDA014242 (UCB INC) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DEXACORT; Active ingredients: DEXAMETHASONE SODIUM PHOSPHATE; Application number: NDA014242.
| Brand name | DEXACORT |
|---|---|
| Active ingredients | DEXAMETHASONE SODIUM PHOSPHATE |
| Application number | NDA014242 |
| Sponsor | UCB INC |
| Dosage form | AEROSOL |
| Route | NASAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19651217 |
| Source | openFDA Drugs@FDA |
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