NDC 69784-231
SODIUM ACETATE
Sodium Acetate
SODIUM ACETATE is a Intravenous Injection, Solution, Concentrate in the Human Prescription Drug category. It is labeled and distributed by Woodward Pharma Services Llc. The primary component is Sodium Acetate.
Product ID | 69784-231_3fee562e-a285-4700-89df-b34185927684 |
NDC | 69784-231 |
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 | 2021-06-01 |
Marketing Category | ANDA / |
Application Number | ANDA214805 |
Labeler Name | Woodward Pharma Services LLC |
Substance Name | SODIUM ACETATE |
Active Ingredient Strength | 164 mg/mL |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |