Drug application

PREDNISOLONE (PREDNISOLONE)

Drugs@FDA ANDA 080562 · FERRANTE

Key facts

Drug name PREDNISOLONE
Active ingredients PREDNISOLONE
Application type ANDA
Application number 080562
Company FERRANTE
Dosage forms TABLET, ORAL
Strength 2.5MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date May 9, 1972

At a glance

  • 1–9 Submissions
  • 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

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