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General MedicationsORALStandard

MINIPRESS

PRAZOSIN HYDROCHLORIDE

Standard Dose
EQ 5MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: PRIORITY Marketing status: Prescription
Summary

Approval overview MINIPRESS is listed in Drugs@FDA under application 017442 (NDA).

Review priority: PRIORITY Marketing status: Prescription Active ingredient PRAZOSIN HYDROCHLORIDE Form and strength CAPSULE;ORAL - EQ 5MG BASE Sponsor PFIZER Submission history Latest submission status date: 2016-01-08 00:00:00.

Structured Monograph

Clinical summary

Approval overview MINIPRESS is listed in Drugs@FDA under application 017442 (NDA). Review priority: PRIORITY Marketing status: Prescription Active ingredient PRAZOSIN HYDROCHLORIDE Form and strength CAPSULE;ORAL - EQ 5MG BASE Sponsor PFIZER Submission history Latest submission status date: 2016-01-08 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Prescription
  • • Review priority: PRIORITY

Interaction Notes

  • No interaction notes stored yet.