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General MedicationsORALGeneric

ZEGERID

MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE

Standard Dose
700MG;40MG;600MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview ZEGERID is listed in Drugs@FDA under application 021850 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE Form and strength TABLET, CHEWABLE;ORAL - 700MG;40MG;600MG Sponsor SANTARUS Submission history Latest submission status date: 2010-09-03 00:00:00.

Structured Monograph

Clinical summary

Approval overview ZEGERID is listed in Drugs@FDA under application 021850 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE Form and strength TABLET, CHEWABLE;ORAL - 700MG;40MG;600MG Sponsor SANTARUS Submission history Latest submission status date: 2010-09-03 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
ZEGERID (MAGNESIUM HYDROXIDE; OMEPRAZOLE; SODIUM BICARBONATE) | Drug Monograph | MedicHelpline