Drug application

RUFINAMIDE (RUFINAMIDE)

Drugs@FDA ANDA 207363 · HIKMA PHARMS

Key facts

Drug name RUFINAMIDE
Active ingredients RUFINAMIDE
Application type ANDA
Application number 207363
Company HIKMA PHARMS
Dosage forms SUSPENSION, ORAL
Strength 40MG/ML
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Apr 23, 2019

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • None Label versions
  • 1–9 Products
  • 1–9 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