Drug application

PREDNISONE (PREDNISONE)

Drugs@FDA ANDA 083807 · PHOENIX LABS NY

Key facts

Drug name PREDNISONE
Active ingredients PREDNISONE
Application type ANDA
Application number 083807
Company PHOENIX LABS NY
Dosage forms TABLET, ORAL
Strength 20MG
Marketing status Discontinued
Reference listed drug No

At a glance

  • None Label versions
  • 1–9 Products
  • None 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