SUBLIMAZE

This brand name is authorized in Ireland, New Zealand, United Kingdom, South Africa

Active ingredients

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

1 Fentanyl
UNII MUN5LYG46H - FENTANYL CITRATE

Fentanyl is a potent ยต-opioid analgesic with rapid onset of analgesia and short duration of action. Its primary therapeutic actions are analgesia and sedation and is approximately 100-fold more potent than morphine as an analgesic. Secondary effects of fentanyl on central nervous system (CNS), respiratory and gastro-intestinal function are typical of opioid analgesics and are considered to be class effects.

Read about Fentanyl

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
SUBLIMAZE Solution for injection Medicines & Healthcare Products Regulatory Agency (GB) 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
N01AH01 Fentanyl N Nervous system → N01 Anesthetics → N01A Anesthetics, general → N01AH Opioid anesthetics
Discover more medicines within N01AH01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 45227
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 1268
Country: ZA Health Products Regulatory Authority Identifier(s): B/2.9/1014, Q/2.9/0034

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