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These highlights do not include all the information needed to use BUPRENORPHINE HYDROCHLORIDE SUBLINGUAL TABLETS safely and effectively. See full prescribing information for BUPRENORPHINE HYDROCHLORIDE SUBLINGUAL TABLETS. BUPRENORPHINE HYDROCHLORIDE sublingual tablets, for sublingual administration CIII 996 997 Initial U.S. Approval: 2002
Medication labelWhy this: Advisory · dailymed-prescription
Buprenorphine hydrochloride sublingual tablets are indicated for the treatment of opioid dependence and are preferred for induction. Buprenorphine hydrochloride sublingual tablets should be used as part of a complete treatment plan to include counseling and psychosocial support. Under the Drug Addiction Treatment Act (DATA) codified at 21 U.S.C. 823(g), prescription use of this product in the treatment of opioid dependence is limited to healthcare providers who meet certain qualifying requirements, and who have notified the Secretary of Health and Human Services (HHS) of their intent to prescribe this product for the treatment of opioid dependence and have been assigned a unique identification number that must be included on every prescription.
- generic_name
- buprenorphine hydrochloride sublingual
- product_names
- buprenorphine hydrochloride sublingual
- ndc
- 67046-996, 67046-997, 0378-0923, 67046-996-30, 0378-0924, 67046-997-30
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en