FENTORA

This brand name is authorized in United States. It is also authorized in Australia, Brazil, Canada, Hong Kong SAR China, Israel.

Active ingredients

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

1	Fentanyl UNII MUN5LYG46H - FENTANYL CITRATE
	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
FENTORA Tablet	MPI, US: SPL/PLR	FDA, National Drug Code (US)

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)
AU	Pharmaceutical Benefits Scheme	10684H, 10697B, 10698C, 10713W, 10722H, 10723J, 10729Q, 10737D, 10738E, 10739F
BR	Câmara de Regulação do Mercado de Medicamentos	537519070007805, 537519070007905, 537519070008005, 537519070008105, 537519070008205, 537519070008305, 537519070008405
CA	Health Products and Food Branch	02408007, 02408015, 02408023, 02408031, 02408058
HK	Department of Health Drug Office	64078, 64079, 64080, 64081, 64082
IL	מִשְׂרַד הַבְּרִיאוּת	7611, 7612, 7613, 7614, 7615
US	FDA, National Drug Code	63459-541, 63459-542, 63459-544, 63459-546, 63459-548