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General MedicationsOPHTHALMICStandard

ROCKLATAN

LATANOPROST; NETARSUDIL DIMESYLATE

Standard Dose
0.005%;EQ 0.02% BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary

Approval overview ROCKLATAN is listed in Drugs@FDA under application 208259 (NDA).

Review priority: STANDARD Marketing status: Prescription Active ingredient LATANOPROST; NETARSUDIL DIMESYLATE Form and strength SOLUTION/DROPS;OPHTHALMIC - 0.005%;EQ 0.02% BASE Sponsor ALCON LABS INC Submission history Latest submission status date: 2025-01-24 00:00:00.

Structured Monograph

Clinical summary

Approval overview ROCKLATAN is listed in Drugs@FDA under application 208259 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient LATANOPROST; NETARSUDIL DIMESYLATE Form and strength SOLUTION/DROPS;OPHTHALMIC - 0.005%;EQ 0.02% BASE Sponsor ALCON LABS INC Submission history Latest submission status date: 2025-01-24 00:00:00. Submission type: SUPPL.

Monitoring

  • • Marketing status: Prescription
  • • Review priority: STANDARD

Interaction Notes

  • No interaction notes stored yet.