General MedicationsORALGeneric

KERLONE

BETAXOLOL HYDROCHLORIDE

Standard Dose

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 KERLONE is listed in Drugs@FDA under application 019507 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient BETAXOLOL HYDROCHLORIDE Form and strength TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2011-08-17 00:00:00.

Structured Monograph

Clinical summary

Approval overview KERLONE is listed in Drugs@FDA under application 019507 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient BETAXOLOL HYDROCHLORIDE Form and strength TABLET;ORAL - 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANOFI AVENTIS US Submission history Latest submission status date: 2011-08-17 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued
• Review priority: STANDARD

Interaction Notes

No interaction notes stored yet.