Drug application

AMIFAMPRIDINE (AMIFAMPRIDINE)

Drugs@FDA ANDA 217996 · LUPIN LIMITED

Key facts

Drug name AMIFAMPRIDINE
Active ingredients AMIFAMPRIDINE
Application type ANDA
Application number 217996
Company LUPIN LIMITED
Dosage forms TABLET
Strength 10MG
Marketing status None (Tentative Approval)
Reference listed drug No
Latest submission status date Mar 12, 2025

At a glance

  • 1–9 Submissions
  • None Label versions
  • None 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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