Drug application

IRBESARTAN AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE, IRBESARTAN)

Drugs@FDA ANDA 203500 · DR REDDYS LABS LTD

Key facts

Drug name IRBESARTAN AND HYDROCHLOROTHIAZIDE
Active ingredients HYDROCHLOROTHIAZIDE, IRBESARTAN
Application type ANDA
Application number 203500
Company DR REDDYS LABS LTD
Dosage forms TABLET, ORAL
Strength 12.5MG;150MG
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Sep 27, 2012

At a glance

  • 1–9 Submissions
  • None Label versions
  • 1–9 Products
  • 10–99 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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