ACTRAPHANE

This brand name is authorized in Austria, Germany, Estonia, Croatia, 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 about Insulin (human)

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
ACTRAPHANE 30 Suspension for injection	European Medicines Agency (EU)	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
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)
Country: DE	Bundesinstitut für Arzneimittel und Medizinprodukte	Identifier(s): 00539650, 00540765, 00541463, 00541486, 00541581, 00541629, 00542356, 00542882
Country: EE	Ravimiamet	Identifier(s): 1203781, 1203792, 1203804, 1203815, 1203893, 1203905, 1203916, 1203949, 1203950, 1203961, 1203972, 1203983, 1203994, 1204007, 1204018, 1204029, 1204030, 1204041, 1204052
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1027164, 1027165, 1027166, 1027167, 1027168, 1027169, 1027198, 1027199, 1027200, 1027201, 1027202, 1027203, 1027204, 1027205, 1027206, 1027218, 1027219, 1027220, 1027221, 1027222, 1027223
Country: NL	Z-Index G-Standaard	Identifier(s): 14816091
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 65994, 66176, 66257
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100308261, 100308284, 100308290, 100308309, 100308315, 100308350, 100308367
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): 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
Country: ZA	Health Products Regulatory Authority	Identifier(s): W/21.1/287