FDA — authorised 17 September 1940
- Marketing authorisation holder: POYTHRESS
- Status: approved
🇺🇸 SULFUR in United States
FDA authorised SULFUR on 17 September 1940
Marketing authorisations
FDA — authorised 17 September 1940
- Application: NDA002918
- Marketing authorisation holder: POYTHRESS
- Local brand name: BENSULFOID
- Indication: POWDER — TOPICAL
- Status: approved
SULFUR in other countries
Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.
Other Immunology approved in United States
Frequently asked questions
Is SULFUR approved in United States?
Yes. FDA authorised it on 17 September 1940; FDA authorised it on 17 September 1940.
Who is the marketing authorisation holder for SULFUR in United States?
POYTHRESS holds the US marketing authorisation.