OSMITROL

This brand name is authorized in Canada, Hong Kong, Mexico, New Zealand, United States

Active ingredients

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

1 Mannitol
UNII 3OWL53L36A - MANNITOL

Mannitol is a naturally occurring sugar alcohol used clinically primarily for its osmotic diuretic properties.

Read about Mannitol

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
OSMITROL Solution for injection FDA, National Drug Code (US) MPI, US: SPL/PLR

Medicine classification

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

ATC code Group title Classification
B05BC01 Mannitol B Blood and blood forming organs → B05 Blood substitutes and perfusion solutions → B05B I.V. solutions → B05BC Solutions producing osmotic diuresis
Discover more medicines within B05BC01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 00060410, 00060437
Country: HK Department of Health Drug Office Identifier(s): 21527
Country: MX Comisiรณn Federal para la Protecciรณn contra Riesgos Sanitarios Identifier(s): 70597
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 3566, 3568
Country: US FDA, National Drug Code Identifier(s): 0338-0353, 0338-0355, 0338-0357

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