TIROFIBAN HYDROCHLORIDE (TIROFIBAN HYDROCHLORIDE) — FDA Approval ANDA213947 (NEXUS)
TIROFIBAN HYDROCHLORIDE (TIROFIBAN HYDROCHLORIDE) — FDA Approval ANDA213947 (NEXUS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: TIROFIBAN HYDROCHLORIDE; Active ingredients: TIROFIBAN HYDROCHLORIDE; Application number: ANDA213947.
| Brand name | TIROFIBAN HYDROCHLORIDE |
|---|---|
| Active ingredients | TIROFIBAN HYDROCHLORIDE |
| Application number | ANDA213947 |
| Sponsor | NEXUS |
| Dosage form | SOLUTION |
| Route | INTRAVENOUS |
| Marketing status | Prescription |
| Products in application | 2 |
| First approval date | 20230207 |
| Source | openFDA Drugs@FDA |
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