Drug application

GALANTAMINE HYDROBROMIDE (GALANTAMINE HYDROBROMIDE)

Drugs@FDA ANDA 078484 · IMPAX LABS

Key facts

Drug name GALANTAMINE HYDROBROMIDE
Active ingredients GALANTAMINE HYDROBROMIDE
Application type ANDA
Application number 078484
Company IMPAX LABS
Dosage forms CAPSULE, EXTENDED RELEASE, ORAL
Strength EQ 8MG BASE
Marketing status Discontinued
Reference listed drug No
Latest submission status date May 27, 2009

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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