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Sodium Acetate
Sodium Acetate - 0409-7299-73 - (SODIUM ACETATE)
Drug Information of Sodium Acetate
| Product NDC: | 0409-7299 |
| Proprietary Name: | Sodium Acetate |
| Non Proprietary Name: | SODIUM ACETATE |
| Active Ingredient(s): | 3.28 g/20mL & nbsp; SODIUM ACETATE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Acetate
| Product NDC: | 0409-7299 |
| Labeler Name: | Hospira, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018893 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110823 |
Package Information of Sodium Acetate
| Package NDC: | 0409-7299-73 |
| Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73) > 20 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Sodium Acetate
| NDC Code | 0409-7299-73 |
| Proprietary Name | Sodium Acetate |
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73) > 20 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0409-7299 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM ACETATE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110823 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM ACETATE |
| Strength Number | 3.28 |
| Strength Unit | g/20mL |
| Pharmaceutical Classes |
