NDC 0264-7780 Ringers

Sodium Chloride,Calcium Chloride,And Potassium Chloride Injection, Solution Intravenous - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0264-7780
Proprietary Name:
Ringers
Non-Proprietary Name: [1]
Sodium Chloride, Calcium Chloride, And Potassium Chloride
Substance Name: [2]
Calcium Chloride; Potassium Chloride; Sodium Chloride
NDC Directory Status:
Human Prescription Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route(s): [4]
  • Intravenous - Administration within or into a vein or veins.
  • Labeler Name: [5]
    B. Braun Medical Inc.
    Labeler Code:
    0264
    FDA Application Number: [6]
    NDA020002
    Marketing Category: [8]
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date: [9]
    04-17-1992
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 0264-7780-00

    Package Description: 12 CONTAINER in 1 CASE / 1000 mL in 1 CONTAINER

    Product Details

    What is NDC 0264-7780?

    The NDC code 0264-7780 is assigned by the FDA to the product Ringers which is a human prescription drug product labeled by B. Braun Medical Inc.. The generic name of Ringers is sodium chloride, calcium chloride, and potassium chloride. The product's dosage form is injection, solution and is administered via intravenous form. The product is distributed in a single package with assigned NDC code 0264-7780-00 12 container in 1 case / 1000 ml in 1 container. 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 Ringers?

    This solution is indicated for use in adults and pediatric patients as a source of electrolytes and water for hydration.

    What are Ringers Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • CALCIUM CHLORIDE .033 g/100mL - A salt used to replenish calcium levels, as an acid-producing diuretic, and as an antidote for magnesium poisoning.
    • POTASSIUM CHLORIDE .03 g/100mL - A white crystal or crystalline powder used in BUFFERS; FERTILIZERS; and EXPLOSIVES. It can be used to replenish ELECTROLYTES and restore WATER-ELECTROLYTE BALANCE in treating HYPOKALEMIA.
    • SODIUM CHLORIDE .86 g/100mL - A ubiquitous sodium salt that is commonly used to season food.

    Which are Ringers UNII Codes?

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

    Which are Ringers 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 Ringers?

    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: 847617 - Ringers Injectable Solution
    • RxCUI: 847617 - calcium chloride 0.33 MG/ML / potassium chloride 0.3 MG/ML / sodium chloride 8.6 MG/ML Injectable Solution
    • RxCUI: 847617 - calcium chloride 0.33 MG/ML / K+ chloride 0.3 MG/ML / NaCl 8.6 MG/ML Injectable Solution
    • RxCUI: 847617 - calcium chloride 0.33 MG/ML / Pot chloride 0.3 MG/ML / NaCl 8.6 MG/ML Injectable Solution
    • RxCUI: 847617 - calcium chloride 33 MG / potassium chloride 30 MG / sodium chloride 860 MG per 100 ML Ringer's Injectable Solution

    Which are the Pharmacologic Classes for Ringers?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

    [8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

    [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".