FDA Approved: BUPRENORPHINE HYDROCHLORIDE — Supplemental Application (PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma)

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Summary

FDA approved a supplemental application for buprenorphine hydrochloride (generic) from PAI Holdings, under ANDA 090622.

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Diseases / indications

• Opioid Use Disorder
• Pain

Drugs mentioned

• Buprenorphine Hydrochloride (Buprenorphine hydrochloride)

Snippet

SUPPL AP for BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)