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FDA approval · 2022-05-03

FDA Approved: BUPRENORPHINE AND NALOXONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)

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Summary

The FDA approved Sun Pharmaceutical's supplemental application for a buprenorphine/naloxone product (ANDA 201633) intended for the treatment of opioid use disor…

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Diseases / indications

Drugs mentioned

  • Buprenorphine and naloxone (BUPRENORPHINE AND NALOXONE)

Snippet

SUPPL AP for BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)