Active substance
Dimethyl sulfoxide
- US FDA 3
- Health Canada 1
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
|---|---|---|---|---|---|
| RIMSO-50 | 50% | solution · intravesical | MYLAN INSTITUTIONAL | Prescription | 4 Apr 1978 |
| DIMETHYL SULFOXIDE | 50% | solution · intravesical | RENOVA PHARMS | Prescription | 7 Jul 2026 |
| DIMETHYL SULFOXIDE | 50% | solution · intravesical | MYLAN INSTITUTIONAL | Discontinued | 29 Nov 2002 |
Canada Canada — marketed products (Health Canada)
| Brand | DIN | Strength | Form · route | Company |
|---|---|---|---|---|
| RIMSO-50 | 00493392 | 500 MG / G | SOLUTION · INTRAVESICAL | MYLAN PHARMACEUTICALS ULC |
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.