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FDA Product

Sodium Thiosulfate

Product approved by U.S. Food and Drug Administration (US)

Basic Information

Sodium Thiosulfate

60267-705

Regulatory Information

60267-705

NDA203923

C73594

November 16, 2023

USA

These highlights do not include all the information needed to use the SODIUM THIOSULFATE INJECTION safely and effectively. See full prescribing information for SODIUM THIOSULFATE INJECTION. Sodium Thiosulfate Injection, USP Initial U.S. Approval: 1992

HUMAN PRESCRIPTION DRUG LABEL

12

Company Information

015227945

Active Ingredients

Sodium Thiosulfate

Quantity: 250 mg in 1 mL

Code: HX1032V43M

Class Code: ACTIB

Nitrogen

Code: N762921K75

Class Code: IACT

Water

Code: 059QF0KO0R

Class Code: IACT

Boric Acid

Quantity: 2.8 mg in 1 mL

Code: R57ZHV85D4

Class Code: IACT

Sodium Hydroxide

Code: 55X04QC32I

Class Code: IACT

Potassium Chloride

Quantity: 4.4 mg in 1 mL

Code: 660YQ98I10

Class Code: IACT

Active Moieties

THIOSULFATE ION

Code: LLT6XV39PY

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