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Sodium Thiosulfate
Sodium Thiosulfate - 60267-705-50 - (Sodium Thiosulfate)
Drug Information of Sodium Thiosulfate
| Product NDC: | 60267-705 |
| Proprietary Name: | Sodium Thiosulfate |
| Non Proprietary Name: | Sodium Thiosulfate |
| Active Ingredient(s): | 250 mg/mL & nbsp; Sodium Thiosulfate |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Thiosulfate
| Product NDC: | 60267-705 |
| Labeler Name: | Hope Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA203923 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120214 |
Package Information of Sodium Thiosulfate
| Package NDC: | 60267-705-50 |
| Package Description: | 50 mL in 1 VIAL, SINGLE-USE (60267-705-50) |
NDC Information of Sodium Thiosulfate
| NDC Code | 60267-705-50 |
| Proprietary Name | Sodium Thiosulfate |
| Package Description | 50 mL in 1 VIAL, SINGLE-USE (60267-705-50) |
| Product NDC | 60267-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Thiosulfate |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120214 |
| Marketing Category Name | NDA |
| Labeler Name | Hope Pharmaceuticals |
| Substance Name | SODIUM THIOSULFATE |
| Strength Number | 250 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
