DIANEAL

This brand name is authorized in Austria, Brazil, Canada, Ecuador, Hong Kong, New Zealand, Singapore, United States

Active ingredients

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

1 Glucose
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 about Glucose
2 Sodium chloride
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 about Sodium chloride
3 Lactic acid
UNII TU7HW0W0QT - SODIUM LACTATE
Read about Lactic acid
4 Calcium chloride
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 about Calcium chloride
5 Magnesium chloride
UNII 02F3473H9O - MAGNESIUM CHLORIDE
Read about Magnesium chloride

Medicine classification

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

ATC code Group title 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)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 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
Country: CA Health Products and Food Branch Identifier(s): 00799793, 00799807, 00799815, 00799823, 00865095, 00865109, 00865117
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 16.861-3-03-12, 16.862-2-11-03, 16.863-2-04-02
Country: HK Department of Health Drug Office Identifier(s): 22004, 22007, 22008, 33172, 35012, 42530, 42531, 42532, 42533, 42534, 42544, 62678, 62679, 62680, 62709, 62710, 62711
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 15785, 15786, 15787, 7255, 7258, 7261, 7265, 7267
Country: SG Health Sciences Authority Identifier(s): 05589P, 05590P, 05748P, 06625P, 06626P, 06627P
Country: US FDA, National Drug Code Identifier(s): 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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