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General MedicationsORALGeneric

LOTENSIN

BENAZEPRIL HYDROCHLORIDE

Standard Dose
5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 LOTENSIN is listed in Drugs@FDA under application 019851 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient BENAZEPRIL HYDROCHLORIDE Form and strength TABLET;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALIDUS PHARMS Submission history Latest submission status date: 2019-01-07 00:00:00.

Structured Monograph

Clinical summary

Approval overview LOTENSIN is listed in Drugs@FDA under application 019851 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient BENAZEPRIL HYDROCHLORIDE Form and strength TABLET;ORAL - 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor VALIDUS PHARMS Submission history Latest submission status date: 2019-01-07 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.