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Sodium Acetate
Sodium Acetate - 63323-032-61 - (SODIUM ACETATE)
Drug Information of Sodium Acetate
| Product NDC: | 63323-032 |
| Proprietary Name: | Sodium Acetate |
| Non Proprietary Name: | SODIUM ACETATE |
| Active Ingredient(s): | 328 mg/100mL & 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: | 63323-032 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20000901 |
Package Information of Sodium Acetate
| Package NDC: | 63323-032-61 |
| Package Description: | 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-61) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
NDC Information of Sodium Acetate
| NDC Code | 63323-032-61 |
| Proprietary Name | Sodium Acetate |
| Package Description | 25 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-61) > 100 mL in 1 VIAL, PHARMACY BULK PACKAGE |
| Product NDC | 63323-032 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM ACETATE |
| Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20000901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | SODIUM ACETATE |
| Strength Number | 328 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes |
