ACTRAPHANE

This brand name is authorized in Austria, Croatia, Estonia, Germany, Ireland, Lithuania, Netherlands, Poland, Romania, South Africa.

Active ingredients

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

1	Insulin (human) UNII 1Y17CTI5SR - INSULIN HUMAN
	The blood glucose lowering effect of insulin is due to the facilitated uptake of glucose following binding of insulin to receptors on muscle and fat cells and to the simultaneous inhibition of glucose output from the liver.
	Read more about Insulin (human)

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
ACTRAPHANE 30 Suspension for injection	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
A10AD01	Insulin (human)	A Alimentary tract and metabolism → A10 Drugs used in diabetes → A10A Insulins and analogues → A10AD Insulins and analogues for injection, intermediate-acting combined with fast-acting
Discover more medicines within A10AD01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	00539650, 00540765, 00541463, 00541486, 00541581, 00541629, 00542356, 00542882
EE	Ravimiamet	1203781, 1203792, 1203804, 1203815, 1203893, 1203905, 1203916, 1203949, 1203950, 1203961, 1203972, 1203983, 1203994, 1204007, 1204018, 1204029, 1204030, 1204041, 1204052
LT	Valstybinė vaistų kontrolės tarnyba	1027164, 1027165, 1027166, 1027167, 1027168, 1027169, 1027198, 1027199, 1027200, 1027201, 1027202, 1027203, 1027204, 1027205, 1027206, 1027218, 1027219, 1027220, 1027221, 1027222, 1027223
NL	Z-Index G-Standaard	14816091
NL	Z-Index G-Standaard, PRK	65994, 66176, 66257
PL	Rejestru Produktów Leczniczych	100308261, 100308284, 100308290, 100308309, 100308315, 100308350, 100308367
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W51802001, W51802002, W51802003, W51803001, W51803002, W51803003, W51804001, W51804002, W51804003, W51805001, W51805002, W51805003, W51806001, W51806002, W51806003, W51807001, W51807002, W51807003, W51808001, W51808002, W51808003, W51809001, W51809002, W51810001, W51810002, W51811001, W51811002, W51812001, W51812002, W51813001, W51813002, W51814001, W51814002, W51814003, W51815001, W51815002, W51815003
ZA	Health Products Regulatory Authority	W/21.1/287