Drug · DIN 02239569
LYTEPREP
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 September 26, 2005; first marketed January 25, 2000.
- Drug Identification Number (DIN)
- 02239569
- Company (DIN owner)
- Therapex Division De E-Z-Em Canada IncVille D'Anjou, Quebec, Canada
- Schedule
- Ethical
- Dosage form
- Powder
- Route
- Oral
- Therapeutic class (ATC)
- Mineral salts in combination A06AD10
- Class
- Human
- Record last updated
- March 22, 2025
Active ingredients
As listed in the Drug Product Database.
| Ingredient | Strength | Per |
|---|---|---|
| POLYETHYLENE GLYCOL 3350 | 236 G | BOTTLE |
| SODIUM SULFATE | 22.74 G | BOTTLE |
| SODIUM BICARBONATE | 6.74 G | BOTTLE |
| SODIUM CHLORIDE | 5.86 G | BOTTLE |
| POTASSIUM CHLORIDE | 2.97 G | BOTTLE |
Other DINs named LYTEPREP
- DIN 00695335 · Cancelled Post Market