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General MedicationsORALGeneric

ESIMIL

GUANETHIDINE MONOSULFATE; HYDROCHLOROTHIAZIDE

Standard Dose
10MG;25MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary

Approval overview ESIMIL is listed in Drugs@FDA under application 013553 (NDA).

Marketing status: Discontinued Active ingredient GUANETHIDINE MONOSULFATE; HYDROCHLOROTHIAZIDE Form and strength TABLET;ORAL - 10MG;25MG Sponsor NOVARTIS Submission history See approval history documents.

Structured Monograph

Clinical summary

Approval overview ESIMIL is listed in Drugs@FDA under application 013553 (NDA). Marketing status: Discontinued Active ingredient GUANETHIDINE MONOSULFATE; HYDROCHLOROTHIAZIDE Form and strength TABLET;ORAL - 10MG;25MG Sponsor NOVARTIS Submission history See approval history documents.

Monitoring

  • • Marketing status: Discontinued

Interaction Notes

  • No interaction notes stored yet.