Drug application

HYDROCODONE BITARTRATE (HYDROCODONE BITARTRATE)

Drugs@FDA ANDA 206952 · ACTAVIS LABS FL INC

Key facts

Drug name HYDROCODONE BITARTRATE
Active ingredients HYDROCODONE BITARTRATE
Application type ANDA
Application number 206952
Company ACTAVIS LABS FL INC
Dosage forms CAPSULE, EXTENDED RELEASE, ORAL
Strength 10MG
Marketing status None (Tentative Approval)
Reference listed drug No
Latest submission status date Apr 5, 2017

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 · Source date:

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