FDA — authorised 12 August 1981
- Application: NDA018485
- Marketing authorisation holder: MT ADAMS
- Local brand name: ISOPTIN
- Indication: INJECTABLE — INJECTION
- Status: approved
FDA authorised Verapamil Injection on 12 August 1981 · 1 US adverse-event reports
Adverse reaction reports describe suspected side effects. A report does not mean the drug caused the event — co-medications, underlying disease and coincidence all contribute.
Yes. FDA authorised it on 12 August 1981; FDA authorised it on 8 March 1982; FDA authorised it on 30 March 1984.
MT ADAMS holds the US marketing authorisation.