Drug application

HALOPERIDOL (HALOPERIDOL)

Drugs@FDA ANDA 071724 · ROYCE LABS

Key facts

Drug name HALOPERIDOL
Active ingredients HALOPERIDOL
Application type ANDA
Application number 071724
Company ROYCE LABS
Dosage forms TABLET, ORAL
Strength 2MG
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

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