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General MedicationsTOPICALGeneric

SOLARAZE

DICLOFENAC SODIUM

Standard Dose
3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 SOLARAZE is listed in Drugs@FDA under application 021005 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient DICLOFENAC SODIUM Form and strength GEL;TOPICAL - 3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor FOUGERA PHARMS Submission history Latest submission status date: 2024-11-21 00:00:00.

Structured Monograph

Clinical summary

Approval overview SOLARAZE is listed in Drugs@FDA under application 021005 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient DICLOFENAC SODIUM Form and strength GEL;TOPICAL - 3% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor FOUGERA PHARMS Submission history Latest submission status date: 2024-11-21 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.
SOLARAZE (DICLOFENAC SODIUM) | Drug Monograph | MedicHelpline