BUVIDAL

This brand name is authorized in the following countries: Austria Australia Estonia Spain Finland Ireland Lithuania New Zealand Poland United Kingdom

Active ingredients

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

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
 
European Medicines Agency (EU)
Summary of Product Characteristics (SPC)

Medicine classification

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

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

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.