Drug application

NIZATIDINE (NIZATIDINE)

Drugs@FDA ANDA 077314 · DR REDDYS LABS LTD

Key facts

Drug name NIZATIDINE
Active ingredients NIZATIDINE
Application type ANDA
Application number 077314
Company DR REDDYS LABS LTD
Dosage forms CAPSULE, ORAL
Strength 150MG
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Sep 15, 2005

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