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