BULNEXO

This brand name is authorized in Croatia

Active ingredients

The drug BULNEXO contains a combination of these active pharmaceutical ingredients (APIs):

1 Buprenorphine
UNII 56W8MW3EN1 - BUPRENORPHINE HYDROCHLORIDE

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

Read about Buprenorphine
2 Naloxone
UNII F850569PQR - NALOXONE HYDROCHLORIDE

Naloxone hydrochloride, a semisynthetic morphine derivative (N-allyl-nor-oxymorphone), is a specific opioid antagonist that acts competitively at opioid receptors. It reveals very high affinity for the opioid receptor sites and therefore displaces both opioid agonists and partial antagonists, such as pentazocine, for example, but also nalorphine.

Read about Naloxone

Medicine classification

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

ATC code Group title Classification
N07BC51 Buprenorphine, combinations N Nervous system → N07 Other nervous system drugs → N07B Drugs used in addictive disorders → N07BC Drugs used in opioid dependence
Discover more medicines within N07BC51

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-065726451, HR-H-396897658

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