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	Comisión Federal para la Protección 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