Skip to main content
MedicHelpLine
Join Free
Verified Professional Network190+ CountriesHIPAA-Aware Platform
Back to Drug Index
General MedicationsORALGeneric

SUPRENZA

PHENTERMINE HYDROCHLORIDE

Standard Dose
37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: STANDARD Marketing status: Discontinued
Summary

Approval overview SUPRENZA is listed in Drugs@FDA under application 202088 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient PHENTERMINE HYDROCHLORIDE Form and strength TABLET, ORALLY DISINTEGRATING;ORAL - 37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor CITIUS PHARMS Submission history Latest submission status date: 2014-02-18 00:00:00.

Structured Monograph

Clinical summary

Approval overview SUPRENZA is listed in Drugs@FDA under application 202088 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient PHENTERMINE HYDROCHLORIDE Form and strength TABLET, ORALLY DISINTEGRATING;ORAL - 37.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor CITIUS PHARMS Submission history Latest submission status date: 2014-02-18 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.