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Sodium Selenite

Generic Name
Sodium Selenite

Overview

No overview information available.

Indication

用于防治缺硒引起的疾病,如克山病,大骨节病等。

Associated Conditions

No associated conditions information available.

Research Report

Published: Oct 30, 2025

A Comprehensive Monograph on Sodium Selenite: Chemical Properties, Pharmacological Profile, and Clinical Significance

1.0 Introduction and Compound Identification

1.1 Overview of Sodium Selenite as an Inorganic Selenium Source

Sodium selenite is an inorganic salt that serves as a primary source of the essential trace element selenium. It is utilized across a spectrum of applications, ranging from a nutraceutical in dietary supplements to a therapeutic agent in clinical and veterinary medicine, and as a component in industrial processes.[1] As a chemical entity, it is defined by the duality of its biological role: selenium is indispensable for human health at low, physiological concentrations, yet it exhibits significant toxicity at higher doses.[4] This narrow therapeutic index is a central theme in its pharmacology and toxicology. In medicine, sodium selenite is investigated for its potential antineoplastic activity, a function that contrasts sharply with its role in maintaining cellular homeostasis, setting the stage for a complex, dose-dependent mechanism of action.[1]

1.2 Comprehensive Chemical and Physical Profile

The anhydrous form of sodium selenite is a well-characterized inorganic compound. It is a white or colorless crystalline solid, though it may also be supplied as a beige powder.[1] There is some discrepancy in the literature regarding its hygroscopic nature; while several sources describe it as a hygroscopic solid that readily absorbs moisture from the air, at least one supplier datasheet indicates it is not.[1] This variability may be attributable to differences in sample purity or experimental conditions and underscores the importance of controlled storage for maintaining the compound's integrity.

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FDA Drug Approvals

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No FDA approvals found for this drug.

EMA Drug Approvals

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HSA Drug Approvals

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No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
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No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
JUNYELT CONCENTRATE FOR SOLUTION FOR INFUSION
N/A
N/A
N/A
2/18/2019

TGA Drug Approvals

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
FUSION AM FORMULA TAB
l & s research corporation
01961152
Tablet - Oral
25 MCG / TAB
12/31/1993
MULTI MINERALS CAPSULES
sisu inc.
00679003
Capsule - Oral
25 MCG / CAP
12/31/1986
ORTI-VITE CAP
seroyal international inc.
00829382
Capsule - Oral
66.67 MCG
12/31/1992

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

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Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

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License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

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Company
Registration Number
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Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

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MA Number
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Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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