Home NDC 60267-705 Sodium Thiosulfate
Product NDC 60267-705
11-digit product format 602670705
Labeler code 60267
Product ID 60267-705_4c4f587f-fb6f-4ce3-a09e-2a6a589b4d2b
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Sodium Thiosulfate
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS
Labeler Hope Pharmaceuticals
Application NDA203923
Marketing category NDA
Marketing start 2012-02-14
Substance SODIUM THIOSULFATE
Active strength 250 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Sodium Thiosulfate
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM THIOSULFATE 250 mg/mL
Harmonized Identifiers# Field, Values table Field Values Unii HX1032V43M Rxcui 237832
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 60267-705-50 Sodium Thiosulfate 50 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 50 15 60267-705-50 NITHIODOTE 50 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 50 mL 250 mg in 1mL 10
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 60267-705 SODIUM THIOSULFATE INJECTION, SOLUTION [HOPE PHARMACEUTICALS] 13 Current NDC, Legacy NDC, 1 package rows 20241228_82f55408-2de9-463d-85e8-b39c3b259f0b.zip 60267-705 NITHIODOTE (SODIUM NITRITE AND SODIUM THIOSULFATE) KIT [HOPE PHARMACEUTICALS] 9 Current NDC, Legacy NDC 20241228_ff4941b3-9901-4aab-adcf-c5327bede34e.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 60267-705-50 60267070550 50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50) 50 ml 2012-02-14 0000-00-00 No No Current