Nexus Pharmaceuticals Inc. Receives FDA Approval for Tirofiban Hydrochloride Injection
Nexus Pharmaceuticals Inc. announced that it has received US Food and Drug Administration (FDA) approval for Tirofiban Hydrochloride Injection in 5mg/100mL single-dose IV-bags.
- Nexus Pharmaceuticals Inc. announced that it has received US Food and Drug Administration (FDA) approval for Tirofiban Hydrochloride Injection in 5mg/100mL single-dose IV-bags.
- Tentative approval has been granted for concentrations of 12.5mg/250mL single-dose IV-bags.
- “Being granted this approval is a milestone for us, but also for patients who want more transparency in the healthcare they receive.
- We eagerly anticipate bringing it to market in the coming months.”
Nexus Pharmaceuticals’ Tirofiban Hydrochloride for Injection will be available in cartons of sole single-dose IV bags.