Drug application

LOTEPREDNOL ETABONATE (LOTEPREDNOL ETABONATE)

Drugs@FDA ANDA 215384 · SUN PHARM

Key facts

Drug name LOTEPREDNOL ETABONATE
Active ingredients LOTEPREDNOL ETABONATE
Application type ANDA
Application number 215384
Company SUN PHARM
Dosage forms GEL, OPHTHALMIC
Strength 0.5%
Marketing status Discontinued
TE codes AB
Reference listed drug No
Latest submission status date Aug 9, 2023

At a glance

  • 1–9 Submissions
  • None Label versions
  • 1–9 Products
  • 10–99 Therapeutic equivalents

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

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