Sodium Acetate is a Intravenous Injection, Solution, Concentrate in the Human Prescription Drug category. It is labeled and distributed by Hospira, Inc.. The primary component is Sodium Acetate Anhydrous.
| Product ID | 0409-3299_32fac08e-7507-4e6c-b362-dc0f77f91d00 |
| NDC | 0409-3299 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Sodium Acetate |
| Generic Name | Sodium Acetate |
| Dosage Form | Injection, Solution, Concentrate |
| Route of Administration | INTRAVENOUS |
| Marketing Start Date | 2013-11-19 |
| Marketing Category | NDA / NDA |
| Application Number | NDA018893 |
| Labeler Name | Hospira, Inc. |
| Substance Name | SODIUM ACETATE ANHYDROUS |
| Active Ingredient Strength | 164 mg/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |
| Marketing Start Date | 2013-11-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-04-30 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-12-05 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-04-06 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-04-06 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-05-16 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2017-12-05 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-04-30 |
| Marketing Category | NDA |
| Application Number | NDA018893 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2005-04-30 |
| Ingredient | Strength |
|---|---|
| SODIUM ACETATE ANHYDROUS | 164 mg/mL |
| SPL SET ID: | abc41ed1-9512-4bea-9295-1a9ca134b6c2 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0409-3299 | Sodium Acetate | sodium acetate |
| 0409-7299 | Sodium Acetate | SODIUM ACETATE |
| 51754-9995 | Sodium Acetate | Sodium Acetate |
| 63323-032 | SODIUM ACETATE | SODIUM ACETATE |
| 69784-230 | SODIUM ACETATE | SODIUM ACETATE |
| 69784-231 | SODIUM ACETATE | SODIUM ACETATE |
| 0517-5023 | Sodum Acetate | Sodium Acetate |