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General MedicationsORALStandard

MOEXIPRIL HYDROCHLORIDE

MOEXIPRIL HYDROCHLORIDE

Standard Dose
15MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Prescription
Summary

Approval overview MOEXIPRIL HYDROCHLORIDE is listed in Drugs@FDA under application 090416 (ANDA).

Marketing status: Prescription Active ingredient MOEXIPRIL HYDROCHLORIDE Form and strength TABLET;ORAL - 15MG Sponsor GLENMARK PHARMS LTD Submission history Latest submission status date: 2015-03-02 00:00:00.

Structured Monograph

Clinical summary

Approval overview MOEXIPRIL HYDROCHLORIDE is listed in Drugs@FDA under application 090416 (ANDA). Marketing status: Prescription Active ingredient MOEXIPRIL HYDROCHLORIDE Form and strength TABLET;ORAL - 15MG Sponsor GLENMARK PHARMS LTD Submission history Latest submission status date: 2015-03-02 00:00:00. Submission type: SUPPL.

Monitoring

  • • Review priority: STANDARD
  • • Marketing status: Prescription

Interaction Notes

  • No interaction notes stored yet.