BUVIDAL

This brand name is authorized in Austria, Australia, Estonia, Spain, Finland, Croatia, Ireland, Lithuania, New Zealand, Poland, United Kingdom

Active ingredients

The drug BUVIDAL contains one active pharmaceutical ingredient (API):

1 Buprenorphine
UNII 40D3SCR4GZ - BUPRENORPHINE

Buprenorphine is an opioid partial agonist/antagonist which attaches itself to the μ (mu) and κ (kappa) receptors of the brain. Its activity in opioid maintenance treatment is attributed to its slowly reversible link with the μ receptors which, over a prolonged period, minimises the need of illicit opioids for patients with opioid dependence.

Read about Buprenorphine

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
BUVIDAL Prolonged-release solution for injection European Medicines Agency (EU) MPI, EU: SmPC

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
N07BC01 Buprenorphine N Nervous system → N07 Other nervous system drugs → N07B Drugs used in addictive disorders → N07BC Drugs used in opioid dependence
Discover more medicines within N07BC01

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 11754P, 11759X, 11766G, 11767H, 11768J, 11773P, 11774Q
Country: EE Ravimiamet Identifier(s): 1783009, 1783010, 1783021, 1783032, 1783043, 1783054, 1783065, 1849248
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1181336001, 1181336002, 1181336003, 1181336004, 1181336005, 1181336006, 1181336007
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 038314, 079803, 126957, 176345, 190471, 199899, 510809, 539928
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 367272, 367281, 367290, 367307, 367324, 367339, 367349
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1086600, 1086601, 1086602, 1086603, 1086604, 1086605, 1086606, 1092686
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 21077, 21078, 21079, 21080, 21081, 21082, 21083
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100416720, 100416737, 100416743, 100416750, 100416766, 100416772, 100416789

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