OSMITROL

This brand name is authorized in United States. It is also authorized in Canada, Hong Kong SAR China, Mexico, New Zealand.

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 more about Mannitol

Medication package inserts

Below package inserts are available for further reading:

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

Medicine classification

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

ATC Group		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)
CA	Health Products and Food Branch	00060410, 00060437
HK	Department of Health Drug Office	21527
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	70597
NZ	Medicines and Medical Devices Safety Authority	3566, 3568
US	FDA, National Drug Code	0338-0353, 0338-0355, 0338-0357