Drug · DIN 00520187
ARKODYNE
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 August 18, 1999; first marketed December 31, 1980.
- Drug Identification Number (DIN)
- 00520187
- Company (DIN owner)
- Laboratoire RomiloLaval, Quebec, Canada
- Schedule
- Non-prescription drugs
- Dosage form
- Lozenge
- Route
- Oral
- Therapeutic class (ATC)
- Various R02AA20
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| BENZOCAINE | 4 MG | LOZ |
| BENZALKONIUM CHLORIDE | 1.5 MG | LOZ |
| OXYQUINOLINE SULFATE | 3 MG | LOZ |