Drug · DIN 00001120
HERPLEX
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 4, 2011; first marketed December 31, 1963.
- Drug Identification Number (DIN)
- 00001120
- Company (DIN owner)
- Allergan IncMarkham, Ontario, Canada
- Schedule
- Prescription
- Dosage form
- Drops
- Route
- Ophthalmic
- Therapeutic class (ATC)
- Idoxuridine S01AD01
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| IDOXURIDINE | .1 % | % |