Drug application

DURYSTA (BIMATOPROST)

Drugs@FDA NDA 211911 · ABBVIE

Key facts

Drug name DURYSTA
Active ingredients BIMATOPROST
Application type NDA
Application number 211911
Company ABBVIE
Dosage forms IMPLANT, OPHTHALMIC
Strength 10MCG
Marketing status Prescription
Reference listed drug Yes
Latest submission class Type 3 - New Dosage Form
Latest submission status date Mar 4, 2020

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • 1–9 Label versions
  • 1–9 Products
  • None Therapeutic equivalents
  • Yes FDA letters on file
  • Yes FDA reviews on file

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About Drugs@FDA applications

Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.

Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date:

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