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FDA approval · 2017-05-23

FDA Approved: BUPRENORPHINE AND NALOXONE — Supplemental Application (Lannett Company, Inc.)

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Summary

The FDA approved a supplemental (ANDA) application for a generic buprenorphine/naloxone product from Lannett Company, Inc.

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Diseases / indications

Drugs mentioned

  • Buprenorphine/naloxone (buprenorphine/naloxone)

Snippet

SUPPL AP for BUPRENORPHINE AND NALOXONE (BUPRENORPHINE AND NALOXONE)