Drug application

HALOBETASOL PROPIONATE AND TAZAROTENE (HALOBETASOL PROPIONATE, TAZAROTENE)

Drugs@FDA ANDA 217190 · SUN PHARMA CANADA

Key facts

Drug name HALOBETASOL PROPIONATE AND TAZAROTENE
Active ingredients HALOBETASOL PROPIONATE, TAZAROTENE
Application type ANDA
Application number 217190
Company SUN PHARMA CANADA
Dosage forms LOTION, TOPICAL
Strength 0.01%;0.045%
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date May 2, 2025

At a glance

  • 1–9 Submissions
  • None Label versions
  • 1–9 Products
  • 1–9 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

Browse all Drugs@FDA applications