General MedicationsORALGeneric

RANEXA

RANOLAZINE

Standard Dose

500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 RANEXA is listed in Drugs@FDA under application 021526 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient RANOLAZINE Form and strength TABLET, EXTENDED RELEASE;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor MENARINI INTL Submission history Latest submission status date: 2019-10-29 00:00:00.

Structured Monograph

Clinical summary

Approval overview RANEXA is listed in Drugs@FDA under application 021526 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient RANOLAZINE Form and strength TABLET, EXTENDED RELEASE;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor MENARINI INTL Submission history Latest submission status date: 2019-10-29 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued
• Review priority: STANDARD

Interaction Notes

No interaction notes stored yet.