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General MedicationsORALGeneric

MINIZIDE

POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE

Standard Dose
0.5MG;EQ 1MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary

Approval overview MINIZIDE is listed in Drugs@FDA under application 017986 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE Form and strength CAPSULE;ORAL - 0.5MG;EQ 1MG BASE Sponsor PFIZER Submission history Latest submission status date: 1994-05-10 00:00:00.

Structured Monograph

Clinical summary

Approval overview MINIZIDE is listed in Drugs@FDA under application 017986 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE Form and strength CAPSULE;ORAL - 0.5MG;EQ 1MG BASE Sponsor PFIZER Submission history Latest submission status date: 1994-05-10 00:00:00. Submission type: SUPPL.

Monitoring

  • Marketing status: Discontinued
  • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.
MINIZIDE (POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE) | Drug Monograph | MedicHelpline