FDA
approval
· 2022-05-03
FDA Approved: BUPRENORPHINE AND NALOXONE — Supplemental Application (Sun Pharmaceutical Industries, Inc.)
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
Snippet
SUPPL AP for BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)