0264-2203 NDC - LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)

Drug Information

Product NDC: 0264-2203

Proprietary Name: Lactated Ringers

Non Proprietary Name: Sodium Chloride, Sodium Lactate, Potassium Chloride, and Calcium Chloride

Active Ingredient(s):
  • .02 g/100mL CALCIUM CHLORIDE;
  • .03 g/100mL POTASSIUM CHLORIDE;
  • .6 g/100mL SODIUM CHLORIDE;
  • .31 g/100mL SODIUM LACTATE


Administration Route(s): IRRIGATION

Dosage Form(s): IRRIGANT

Pharmacy Class(es):
  • Blood Coagulation Factor [EPC];
  • Calcium [CS];
  • Cations;
  • Divalent [CS];
  • Increased Coagulation Factor Activity [PE];
  • Increased Large Intestinal Motility [PE];
  • Increased Large Intestinal Motility [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Osmotic Activity [MoA];
  • Osmotic Activity [MoA];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Osmotic Laxative [EPC];
  • Osmotic Laxative [EPC];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC]

Labeler Information

Labeler Name: B. Braun Medical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018681
Marketing Category: NDA
Start Marketing Date:12/27/1982

Package Information

No. Package Code Package Description Billing Unit
10264-2203-0016 CONTAINER in 1 CASE (0264-2203-00) / 1000 mL in 1 CONTAINERML
20264-2203-508 CONTAINER in 1 CASE (0264-2203-50) / 2000 mL in 1 CONTAINERML
30264-2203-704 CONTAINER in 1 CASE (0264-2203-70) / 4000 mL in 1 CONTAINERML

NDC Record

Field Name Field Value Definition
PRODUCT NDC0264-2203The 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.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates 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.
PROPRIETARY NAMELactated RingersThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESodium Chloride, Sodium Lactate, Potassium Chloride, and Calcium ChlorideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEIRRIGANTThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEIRRIGATIONThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE12/27/1982This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMENDAProduct 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.
APPLICATION NUMBERNDA018681This 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.
LABELER NAMEB. Braun Medical Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATEAn 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.
ACTIVE NUMERATOR STRENGTH.02; .03; .6; .31 
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL; g/100mL 
PHARM CLASSESBlood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] 

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