DIANEAL

This brand name is authorized in United States. It is also authorized in Austria, Brazil, Canada, Ecuador, Hong Kong SAR China, New Zealand, Singapore.

Active ingredients

The drug DIANEAL contains a combination of these active pharmaceutical ingredients (APIs):

1
UNII LX22YL083G - DEXTROSE MONOHYDRATE
 

Glucose is frequently used in both adults and children to restore blood glucose concentrations in the treatment of hypoglycaemia resulting from insulin excess or from other causes. The metabolism of glucose is an energy source for the body.

 
Read more about Glucose
2
UNII 451W47IQ8X - SODIUM CHLORIDE
 

Sodium chloride is the principle salt involved in maintaining the osmotic tension of blood and tissues. Changes in osmotic tension influence the movement of fluids and diffusion of salts in cellular tissue.

 
Read more about Sodium chloride
3
UNII TU7HW0W0QT - SODIUM LACTATE
 
Read more about Lactic acid
4
UNII M4I0D6VV5M - CALCIUM CHLORIDE
 

Calcium is the most abundant mineral in the body, and is an essential body electrolyte. Homeostasis is mainly regulated by the parathyroid hormone, by calcitonin, and by the activated form of vitamin D. Calcium is a structural component of bones and teeth. It is also required for blood clotting, neurotransmitter release, muscle contraction and normal heartbeat.

 
Read more about Calcium chloride
5
UNII 02F3473H9O - MAGNESIUM CHLORIDE
 
Read more about Magnesium chloride

Medicine classification

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

ATC Group Classification
B05ZA Hemodialytics, concentrates B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05Z Hemodialytics and hemofiltrates
Discover more medicines within B05ZA

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 503200902152316, 503200903159314, 503200905151310, 503200908150315, 503200909157313, 503200910155310, 503200911151319, 503201201158316, 503201203150312, 503201301152311, 503201302159318, 503201303155316, 503201304151314, 503201402153311, 503201501151317, 503201502158315, 503201503154313, 503201504150311, 503201505157311, 503201506153318, 503201507151319, 503201508156314, 503219010030203, 503219010030303, 503219010030403, 503220090030307, 503220090030407, 503220090030507, 503220110030907
CA Health Products and Food Branch 00799793, 00799807, 00799815, 00799823, 00865095, 00865109, 00865117
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 16.861-3-03-12, 16.862-2-11-03, 16.863-2-04-02
HK Department of Health Drug Office 22004, 22007, 22008, 33172, 35012, 42530, 42531, 42532, 42533, 42534, 42544, 62678, 62679, 62680, 62709, 62710, 62711
NZ Medicines and Medical Devices Safety Authority 15785, 15786, 15787, 7255, 7258, 7261, 7265, 7267
SG Health Sciences Authority 05589P, 05590P, 05748P, 06625P, 06626P, 06627P
US FDA, National Drug Code 0941-0409, 0941-0411, 0941-0413, 0941-0415, 0941-0424, 0941-0426, 0941-0427, 0941-0429, 0941-0430, 0941-0433, 0941-0457, 0941-0459, 0941-0484, 0941-0487, 0941-0490

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