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General MedicationsOPHTHALMICGeneric

OPTIVAR

AZELASTINE HYDROCHLORIDE

Standard Dose
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 OPTIVAR is listed in Drugs@FDA under application 021127 (NDA).

Review priority: STANDARD Marketing status: Discontinued Active ingredient AZELASTINE HYDROCHLORIDE Form and strength SOLUTION/DROPS;OPHTHALMIC - 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor RISING Submission history Latest submission status date: 2025-09-18 00:00:00.

Structured Monograph

Clinical summary

Approval overview OPTIVAR is listed in Drugs@FDA under application 021127 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient AZELASTINE HYDROCHLORIDE Form and strength SOLUTION/DROPS;OPHTHALMIC - 0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Sponsor RISING Submission history Latest submission status date: 2025-09-18 00:00:00. Submission type: SUPPL.

Monitoring

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

Interaction Notes

  • No interaction notes stored yet.