NDC 17856-0595 Sodium Citrate And Citric Acid

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
17856-0595
Proprietary Name:
Sodium Citrate And Citric Acid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Atlantic Biologicals Corp.
Labeler Code:
17856
Start Marketing Date: [9]
01-01-1969
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 17856-0595-4

Package Description: 1 CASE in 1 CUP, UNIT-DOSE / 50 CUP in 1 CASE (17856-0595-3) / 30 mL in 1 CUP

NDC Code 17856-0595-5

Package Description: 1 CASE in 1 CUP, UNIT-DOSE / 72 CUP, UNIT-DOSE in 1 CASE (17856-0595-1) / 15 mL in 1 CUP, UNIT-DOSE

Product Details

What is NDC 17856-0595?

The NDC code 17856-0595 is assigned by the FDA to the product Sodium Citrate And Citric Acid which is product labeled by Atlantic Biologicals Corp.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 17856-0595-4 1 case in 1 cup, unit-dose / 50 cup in 1 case (17856-0595-3) / 30 ml in 1 cup, 17856-0595-5 1 case in 1 cup, unit-dose / 72 cup, unit-dose in 1 case (17856-0595-1) / 15 ml in 1 cup, unit-dose. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Sodium Citrate And Citric Acid?

Sodium Citrate and Citric Acid Oral Solution USP is an effective alkalinizing agent. It is useful in those conditions where long-term maintenance of an alkaline urine is desirable, and is of value in the alleviation of chronic metabolic acidosis, such as results from chronic renal insufficiency or the syndrome of renal tubular acidosis, especially when the administration of potassium salts is undesirable or contraindicated. This product is also useful for buffering and neutralizing gastric hydrochloric acid quickly and effectively.Sodium Citrate and Citric Acid Oral Solution USP is concentrated, and when administered after meals and before bedtime, allows one to maintain an alkaline urinary pH around the clock, usually without the necessity of a 2 A.M. dose. This product alkalinizes the urine without producing a systemic alkalosis in the recommended dosage. This product is highly palatable, pleasant tasting, and tolerable, even when administered for long periods.

Which are Sodium Citrate And Citric Acid UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Sodium Citrate And Citric Acid Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Sodium Citrate And Citric Acid?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 543014 - citric acid 334 MG / sodium citrate 500 MG in 5 mL Oral Solution
  • RxCUI: 543014 - citric acid 66.8 MG/ML / sodium citrate 100 MG/ML Oral Solution
  • RxCUI: 543014 - citric acid 334 MG / sodium citrate 500 MG per 5 ML Oral Solution

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".