Drug · DIN 02423049
REVOLADE
No: cancelled before it was sold
Authorized, then cancelled before it was ever sold in Canada.
Status Cancelled Pre Market since March 11, 2020.
- Drug Identification Number (DIN)
- 02423049
- Company (DIN owner)
- Novartis Pharmaceuticals Canada Inc.Montreal, Quebec, Canada
- Schedule
- Prescription
- Dosage form
- Tablet
- Route
- Oral
- Therapeutic class (ATC)
- Eltrombopag B02BX05
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| ELTROMBOPAG (ELTROMBOPAG OLAMINE) | 75 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- July 30, 2015: NOC 17147New Drug Submission (NDS) · Transfer of Drug Identification Number(s)
- March 27, 2014: NOC 15516Supplement to a New Drug Submission (SNDS) · Addition of new strength - 75 mg tablet. addition of new indication; to increase platelet counts in thrombocytopenic patients with chronic hepatgitis C virus (hcv)
Other DINs named REVOLADE
- DIN 02361825 · Marketed
- DIN 02361833 · Marketed
- DIN 02461382 · Cancelled Pre Market