Drug application

BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)

Drugs@FDA ANDA 078633 · HIKMA PHARMS

Key facts

Drug name BUPRENORPHINE HYDROCHLORIDE
Active ingredients BUPRENORPHINE HYDROCHLORIDE
Application type ANDA
Application number 078633
Company HIKMA PHARMS
Dosage forms TABLET, SUBLINGUAL
Strength EQ 2MG BASE
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Oct 8, 2009

At a glance

  • 1–9 Submissions
  • 10–99 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