NDC 60267-705

Sodium Thiosulfate

Sodium Thiosulfate

Sodium Thiosulfate is a Intravenous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Hope Pharmaceuticals. The primary component is Sodium Thiosulfate.

• Product ID: 60267-705_29449d76-f4c7-4571-b7bb-5c2a55f637b5
• NDC: 60267-705
• Product Type: Human Prescription Drug
• Proprietary Name: Sodium Thiosulfate
• Generic Name: Sodium Thiosulfate
• Dosage Form: Injection, Solution
• Route of Administration: INTRAVENOUS
• Marketing Start Date: 2012-02-14
• Marketing Category: NDA / NDA
• Application Number: NDA203923
• Labeler Name: Hope Pharmaceuticals
• Substance Name: SODIUM THIOSULFATE
• Active Ingredient Strength: 250 mg/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2021-12-31

Packaging

NDC 60267-705-50

50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50)

• Marketing Start Date: 2012-02-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 60267-705-50 [60267070550]

Sodium Thiosulfate INJECTION, SOLUTION

• Marketing Category: NDA
• Application Number: NDA203923
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: ML
• Marketing Start Date: 2012-02-14

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM THIOSULFATE	250 mg/mL

OpenFDA Data

• SPL SET ID: 82f55408-2de9-463d-85e8-b39c3b259f0b
• Manufacturer:
  • Hope Pharmaceuticals
• UNII:
  • HX1032V43M
• RxNorm Concept Unique ID - RxCUI:
  • 237832

NDC Crossover Matching brand name "Sodium Thiosulfate" or generic name "Sodium Thiosulfate"

NDC	Brand Name	Generic Name
60267-705	Sodium Thiosulfate	Sodium Thiosulfate
73077-010	PEDMARK	SODIUM THIOSULFATE