OCL
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE
Approval overview OCL is listed in Drugs@FDA under application 019284 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE Form and strength SOLUTION;ORAL - 6GM/100ML;75MG/100ML;168MG/100ML;146MG/100ML;1.29GM/100ML Sponsor HOSPIRA Submission history Latest submission status date: 2007-12-07 00:00:00.
Structured Monograph
Clinical summary
Approval overview OCL is listed in Drugs@FDA under application 019284 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE Form and strength SOLUTION;ORAL - 6GM/100ML;75MG/100ML;168MG/100ML;146MG/100ML;1.29GM/100ML Sponsor HOSPIRA Submission history Latest submission status date: 2007-12-07 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.