General MedicationsORALStandard

MOEXIPRIL HYDROCHLORIDE

Standard Dose

7.5MG

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 - 7.5MG 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 - 7.5MG 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.