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General MedicationsORALGeneric

SECTRAL

ACEBUTOLOL HYDROCHLORIDE

Standard Dose
EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Max Dose
Refer to approved labeling
Primary Use
Review priority: UNKNOWN Marketing status: Discontinued
Summary

Approval overview SECTRAL is listed in Drugs@FDA under application 018917 (NDA).

Review priority: UNKNOWN Marketing status: Discontinued Active ingredient ACEBUTOLOL HYDROCHLORIDE Form and strength CAPSULE;ORAL - EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor PROMIUS PHARMA Submission history Latest submission status date: 2011-03-03 00:00:00.

Structured Monograph

Clinical summary

Approval overview SECTRAL is listed in Drugs@FDA under application 018917 (NDA). Review priority: UNKNOWN Marketing status: Discontinued Active ingredient ACEBUTOLOL HYDROCHLORIDE Form and strength CAPSULE;ORAL - EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor PROMIUS PHARMA Submission history Latest submission status date: 2011-03-03 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: UNKNOWN

Interaction Notes

  • No interaction notes stored yet.