Drug application

OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN, OXYCODONE HYDROCHLORIDE)

Drugs@FDA ANDA 040789 · AMNEAL PHARMS NY

Key facts

Drug name OXYCODONE AND ACETAMINOPHEN
Active ingredients ACETAMINOPHEN, OXYCODONE HYDROCHLORIDE
Application type ANDA
Application number 040789
Company AMNEAL PHARMS NY
Dosage forms TABLET, ORAL
Strength 500MG;7.5MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date Nov 27, 2007

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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