0517-5023 NDC - SODUM ACETATE ()

Drug Information

Product NDC: 0517-5023

Proprietary Name: Sodum Acetate

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: American Regent, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/30/1990

Package Information

No. Package Code Package Description Billing Unit
10517-5023-2525 VIAL, SINGLE-DOSE in 1 TRAY (0517-5023-25) / 50 mL in 1 VIAL, SINGLE-DOSEML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0517-5023The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMESodum AcetateThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/30/1990This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAmerican Regent, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023