MedPath

Sodium iodide

Generic Name
Sodium iodide
Brand Names
Sclerodine
Drug Type
Small Molecule
Chemical Formula
INa
CAS Number
7681-82-5
Unique Ingredient Identifier
F5WR8N145C

Overview

Sodium iodide is a water-soluble ionic compound with a crystal lattice. Sodium iodide is a source of iodine and can be administered as a supplement for total parenteral nutrition but is more commonly used in veterinary medicine. Radiolabelled compound, Iodide I-131, is used as a diagnostic tool to evaluate thyroid function and morphology.

Indication

Indicated for use as a supplement to intravenous solutions given for total parenteral nutrition (TPN) .

Associated Conditions

  • Abscesses
  • Bleeding of the Vitreal Body
  • Clouding of the Lenses
  • Vitreous opacities
  • Wound

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Perrigo Direct, Inc.
50804-088
TOPICAL
20.4 mg in 1 mL
9/17/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
ANSTO - Sodium Iodide [131I] Therapy Capsules (50 to 6000 MBq)
SIN16117P
CAPSULE
50 to 6000 MBq/capsule
3/8/2021
SODIUM IODIDE NA131I POLATOM CAPSULE
SIN15467P
CAPSULE
37-5500 MBq
4/23/2018

NMPA Drug Approvals

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

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
SODIUM IODIDE INJ 100MG/ML
sabex inc
00807680
Liquid - Intravenous
100 MG / ML
12/31/1988
SCLERODINE 6 INJECTION
omega laboratories limited
02020793
Liquid - Intravenous
90 MG / ML
12/31/1977
NATRUM IODATUM GRAN AND GLOB 5CH-30CH
dolisos laboratoires s.a.
00747157
Tablet - Oral
1 DH / TAB
12/31/1987
PARAMETTES ADULTS
whitehall-robins inc.
02031604
Tablet - Oral
.2 MG / TAB
12/31/1993
NATRUM IODATUM DROPS 5CH-30CH
dolisos laboratoires s.a.
00747165
Drops - Oral
1 DH / DH
12/31/1987

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

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

Saudi SFDA Drug Approvals

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

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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