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General MedicationsDELAYED RELEASEGeneric

POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL

POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL

Standard Dose
2MG; 5MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: None (Tentative Approval)
Summary

Approval overview POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL is listed in Drugs@FDA under application 090197 (ANDA).

Marketing status: None (Tentative Approval) Active ingredient POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL Form and strength SOLUTION; ORAL AND TABLET; DELAYED RELEASE - 2MG; 5MG Sponsor NOVEL LABS INC Submission history Latest submission status date: 2010-05-27 00:00:00.

Structured Monograph

Clinical summary

Approval overview POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL is listed in Drugs@FDA under application 090197 (ANDA). Marketing status: None (Tentative Approval) Active ingredient POLYETHYLENE GLYCOL 3350; SODIUM CHLORIDE; SODIUM BICARBONATE; POTASSIUM CHLORIDE; BISACODYL Form and strength SOLUTION; ORAL AND TABLET; DELAYED RELEASE - 2MG; 5MG Sponsor NOVEL LABS INC Submission history Latest submission status date: 2010-05-27 00:00:00. Submission type: ORIG.

Monitoring

  • Marketing status: None (Tentative Approval)

Interaction Notes

  • No interaction notes stored yet.