Drug application

TAPENTADOL (TAPENTADOL)

Drugs@FDA ANDA 204971 · ACTAVIS ELIZABETH

Key facts

Drug name TAPENTADOL
Active ingredients TAPENTADOL
Application type ANDA
Application number 204971
Company ACTAVIS ELIZABETH
Dosage forms TABLET, ORAL
Strength 50MG
Marketing status None (Tentative Approval)
Reference listed drug No
Latest submission status date May 18, 2015

At a glance

  • 1–9 Submissions
  • 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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