ZOLOFT (SERTRALINE HYDROCHLORIDE) — FDA Approval NDA020990 (VIATRIS)
ZOLOFT (SERTRALINE HYDROCHLORIDE) — FDA Approval NDA020990 (VIATRIS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: ZOLOFT; Active ingredients: SERTRALINE HYDROCHLORIDE; Application number: NDA020990.
| Brand name | ZOLOFT |
|---|---|
| Active ingredients | SERTRALINE HYDROCHLORIDE |
| Application number | NDA020990 |
| Sponsor | VIATRIS |
| Dosage form | CONCENTRATE |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 1 |
| First approval date | 19991207 |
| Source | openFDA Drugs@FDA |
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