FLUOXETINE HYDROCHLORIDE (FLUOXETINE HYDROCHLORIDE) — FDA Approval NDA202133 (TWI PHARMS)
FLUOXETINE HYDROCHLORIDE (FLUOXETINE HYDROCHLORIDE) — FDA Approval NDA202133 (TWI PHARMS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: FLUOXETINE HYDROCHLORIDE; Active ingredients: FLUOXETINE HYDROCHLORIDE; Application number: NDA202133.
| Brand name | FLUOXETINE HYDROCHLORIDE |
|---|---|
| Active ingredients | FLUOXETINE HYDROCHLORIDE |
| Application number | NDA202133 |
| Sponsor | TWI PHARMS |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20111006 |
| Source | openFDA Drugs@FDA |
$1499/mo
Try DrugApprovals →