Drug · DIN 02293501
ADVICOR
No: no longer authorized
The company stopped selling it and its DIN was cancelled. A cancellation is most often a business decision; the record does not say why.
Status Cancelled Post Market since July 26, 2010; first marketed May 15, 2007.
- Drug Identification Number (DIN)
- 02293501
- Company (DIN owner)
- Sepracor Pharmaceuticals IncMississauga, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Tablet (Extended-Release); Tablet (Immediate-Release)
- Route
- Oral
- Therapeutic class (ATC)
- Lovastatin and nicotinic acid C10BA01
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| NICOTINIC ACID | 1000 MG | |
| LOVASTATIN | 40 MG |
Notices of Compliance
Health Canada approvals that name this DIN.
- July 19, 2010: NOC 11601New Drug Submission (NDS) · Manufacturer name change
- March 29, 2007: NOC 8681Supplement to a New Drug Submission (SNDS) · New strengths: 750/20 mg and 1000/40 mg, new maximum daily dose: 2000/40 mg and other revisions to the product monograph
Other DINs named ADVICOR
- DIN 02270439 · Cancelled Post Market
- DIN 02270447 · Cancelled Post Market