PECFENT

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, Spain, UK.

Active ingredients

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

1	Fentanyl UNII UF599785JZ - FENTANYL
	Fentanyl is a potent µ-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 more about Fentanyl

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
PECFENT Nasal spray, solution	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

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

ATC Group		Classification
N02AB03	Fentanyl	N Nervous system → N02 Analgesics → N02A Opioids → N02AB Phenylpiperidine derivatives
Discover more medicines within N02AB03

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1494367, 1494378, 1494389, 1494390, 1595437, 1595448, 1746794
ES	Centro de información online de medicamentos de la AEMPS	10644001, 10644002, 10644003, 10644004
FI	Lääkealan turvallisuus- ja kehittämiskeskus	400789, 597353
FR	Base de données publique des médicaments	66332028, 68001856
GB	Medicines & Healthcare Products Regulatory Agency	176681, 176682, 176686, 176687
HK	Department of Health Drug Office	65413, 65414
IL	מִשְׂרַד הַבְּרִיאוּת	8350, 8351
IT	Agenzia del Farmaco	040328015, 040328027, 040328039, 040328041
LT	Valstybinė vaistų kontrolės tarnyba	1056325, 1056326, 1056327, 1056328, 1064242, 1064243, 1081230
NL	Z-Index G-Standaard, PRK	125660, 125679
PL	Rejestru Produktów Leczniczych	100273628, 100273634
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W69031001, W69031002, W69032001, W69032002