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

TENORMIN

ATENOLOL

Standard Dose
0.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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: PRIORITY Marketing status: Discontinued
Summary

Approval overview TENORMIN is listed in Drugs@FDA under application 019058 (NDA).

Review priority: PRIORITY Marketing status: Discontinued Active ingredient ATENOLOL Form and strength INJECTABLE;INJECTION - 0.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ASTRAZENECA Submission history Latest submission status date: 2005-02-09 00:00:00.

Structured Monograph

Clinical summary

Approval overview TENORMIN is listed in Drugs@FDA under application 019058 (NDA). Review priority: PRIORITY Marketing status: Discontinued Active ingredient ATENOLOL Form and strength INJECTABLE;INJECTION - 0.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ASTRAZENECA Submission history Latest submission status date: 2005-02-09 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Discontinued
  • • Review priority: PRIORITY

Interaction Notes

  • No interaction notes stored yet.