FDA — authorised 24 December 1985
- Application: NDA018972
- Marketing authorisation holder: WYETH PHARMS
- Local brand name: CORDARONE
- Indication: TABLET — ORAL
- Status: approved
🇺🇸 Amiodarone in Parenteral Dosage Form in United States
FDA authorised Amiodarone in Parenteral Dosage Form on 24 December 1985
Marketing authorisations
FDA
- Status: approved
Amiodarone in Parenteral Dosage Form in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Frequently asked questions
Is Amiodarone in Parenteral Dosage Form approved in United States?
Yes. FDA authorised it on 24 December 1985; FDA has authorised it.
Who is the marketing authorisation holder for Amiodarone in Parenteral Dosage Form in United States?
WYETH PHARMS holds the US marketing authorisation.