Drug application

VERAPAMIL HYDROCHLORIDE (VERAPAMIL HYDROCHLORIDE)

Drugs@FDA ANDA 078306 · RISING

Key facts

Drug name VERAPAMIL HYDROCHLORIDE
Active ingredients VERAPAMIL HYDROCHLORIDE
Application type ANDA
Application number 078306
Company RISING
Dosage forms CAPSULE, EXTENDED RELEASE, ORAL
Strength 100MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date Aug 9, 2007

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • None Label versions
  • 1–9 Products
  • None Therapeutic equivalents
  • Yes FDA letters on file
  • No FDA reviews on file

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 · Source date:

Browse all Drugs@FDA applications