Drug application

NADOLOL (NADOLOL)

Drugs@FDA ANDA 210786 · INGENUS PHARMS LLC

Key facts

Drug name NADOLOL
Active ingredients NADOLOL
Application type ANDA
Application number 210786
Company INGENUS PHARMS LLC
Dosage forms TABLET, ORAL
Strength 20MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date Jun 1, 2018

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • 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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