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General MedicationsOPHTHALMICGeneric

IQUIX

LEVOFLOXACIN

Standard Dose
1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 IQUIX is listed in Drugs@FDA under application 021571 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient LEVOFLOXACIN Form and strength SOLUTION/DROPS;OPHTHALMIC - 1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANTEN Submission history Latest submission status date: 2014-12-03 00:00:00.

Structured Monograph

Clinical summary

Approval overview IQUIX is listed in Drugs@FDA under application 021571 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient LEVOFLOXACIN Form and strength SOLUTION/DROPS;OPHTHALMIC - 1.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor SANTEN Submission history Latest submission status date: 2014-12-03 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.