CLENZ-LYTE
POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE
Approval overview CLENZ-LYTE is listed in Drugs@FDA under application 090769 (ANDA).
Marketing status: Discontinued Active ingredient POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE Form and strength FOR SOLUTION;ORAL - 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT Sponsor PADDOCK LLC Submission history Latest submission status date: 2010-06-07 00:00:00.
Structured Monograph
Clinical summary
Approval overview CLENZ-LYTE is listed in Drugs@FDA under application 090769 (ANDA). Marketing status: Discontinued Active ingredient POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM SULFATE Form and strength FOR SOLUTION;ORAL - 236GM/BOT;2.97GM/BOT;6.74GM/BOT;5.86GM/BOT;22.74GM/BOT Sponsor PADDOCK LLC Submission history Latest submission status date: 2010-06-07 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.