Drug application

ALFUZOSIN HYDROCHLORIDE (ALFUZOSIN HYDROCHLORIDE)

Drugs@FDA ANDA 079060 · AUROBINDO PHARMA LTD

Key facts

Drug name ALFUZOSIN HYDROCHLORIDE
Active ingredients ALFUZOSIN HYDROCHLORIDE
Application type ANDA
Application number 079060
Company AUROBINDO PHARMA LTD
Dosage forms TABLET, EXTENDED RELEASE, ORAL
Strength 10MG
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Aug 30, 2012

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • 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

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