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🇪🇺EU · EMAAuthorisedATC: N07BC01

Buprenorphine Neuraxpharm(buprenorphine hydrochloride)

Opioid-Related Disorders

Marketing Authorisation Holder: Neuraxpharm Pharmaceuticals S.L.

EMA Authorisation: 19/12/2024

INN: buprenorphine

Indication

Substitution treatment of opioid drug dependence, within a comprehensive therapeutic monitoring framework of medical, social and psychological treatment. Treatment is intended for use in adults and adolescents 15 years of age and older, who have agreed to be treated for addiction.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.