BUVIDAL

This brand name is authorized in Austria, Australia, Estonia, Spain, Finland, 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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