General MedicationsORALGeneric

TOLECTIN DS

TOLMETIN SODIUM

Standard Dose

EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 TOLECTIN DS is listed in Drugs@FDA under application 018084 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient TOLMETIN SODIUM Form and strength CAPSULE;ORAL - EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ORTHO MCNEIL JANSSEN Submission history Latest submission status date: 2008-01-22 00:00:00.

Structured Monograph

Clinical summary

Approval overview TOLECTIN DS is listed in Drugs@FDA under application 018084 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient TOLMETIN SODIUM Form and strength CAPSULE;ORAL - EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor ORTHO MCNEIL JANSSEN Submission history Latest submission status date: 2008-01-22 00:00:00. Submission type: SUPPL.

Monitoring

• Marketing status: Discontinued
• Review priority: STANDARD

Interaction Notes

No interaction notes stored yet.