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Animal NDC 57699-803-60 Lactated Ringers

Animal Product Information

Field Name Field Value
Animal NDC Code 57699-803-60
Proprietary Name Lactated Ringers What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name Lactated Ringers 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.
Labeler Name A & G Pharmaceuticals, Inc.
Product Type Prescription Animal Drug
Usage Information
    For the correction of electrolyte depletion, metabolic acidosis and dehydration of cattle, calves, horses, sheep and swine.
Active Ingredient(s)
  • Sodium Lactate
  • Sodium Chloride
  • Potassium Chloride
  • Calcium Chloride
Marketing Category UNAPPROVED DRUG OTHER 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.

Lactated Ringers Images

Lactated Ringers Animal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Precautions



CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.
FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN
NET CONTENTS: 1000 mL

CAUTION: Solution should be warmed to body temperature prior to administration and administered at a slow rate. This is a single dose unit. It contains no preservatives. Use entire contents when first opened. 


Indications:




For the correction of electrolyte depletion, metabolic acidosis and dehydration of cattle, calves, horses, sheep and swine.


Dosage & Administration



DOSAGE AND ADMINISTRATION: May be injected intravenously, subcutaneously or intraperitoneally (except in horses) using strict aseptic technique.

Cattle and Horses: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.

Swine and Sheep: 2 to 5 mL per pound of body weight depending on size and condition of animal, repeated 1 to 3 times daily or as needed.

If administered subcutaneously divide the dosage into several sites of injection and massage points of injection to aid in absorption and help prevent inflammation and/or sloughing.


Storage And Handling



Store between 15 degrees C - 30 degrees C (59 degrees F - 86 degrees F)

Dosage Forms & Strengths



EACH 100 mL CONTAINS:

Sodium Chloride....................600 mg

Sodium Lactate.....................310 mg

Potassium Chloride.................30 mg

Calcium Chloride Dihydrate......20 mg

Water for Injection.......................q.s.

The Calcium, Potassium and Sodium contents are approximately 2.7, 4.0 and 130 mEq/liter, respectively. Total Osmolar Concentration: 269 mOsmol per liter (calculated).



Warnings



WARNING: Do not administer to horses by intraperitoneal injection. Do not administer to animals with inadequate renal function. Not for use in lactic acidosis.


Information For Owners/Caregivers



Manufactured by

Nova-Tech, Inc.

Grand Island, NE 68801

TAKE TIME OBSERVE LABEL DIRECTIONS

Iss. 04-09

Manufactured for:

A and G Pharmaceuticals

Clarksburg, NJ 08510




Package Label.Principal Display Panel




* The information on this page is for an ANIMAL PRODUCT, please review the complete disclaimer below.