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Animal NDC 65207-819-25 Sodium Iodide

Animal Product Information

Field Name Field Value
Animal NDC Code 65207-819-25
Proprietary Name Sodium Iodide 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 Sodium Iodide 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 Nova-tech, Inc.
Product Type Prescription Animal Drug
Usage Information
    For use as an aid in the treatment of actinomycosis (lumpy jaw), actinobacillosis (wooden tongue) and necrotic stomatitis in cattle.
Active Ingredient(s)
  • Sodium Iodide
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.

Sodium Iodide Images

Sodium Iodide 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



Indications



For use as an aid in the treatment of actinomycosis (lumpy jaw), actinobacillosis (wooden tongue) and necrotic stomatitis in cattle.


Contraindications



The use of sodium iodide is contraindicated in pregnancy and hyperthyroidism.


Caution



Animals vary in their susceptibility of iodides. Administer with caution until the animal's tolerance is determined. Discontinue treatment if adverse reactions occur.


Dosage And Administration:



Using aspetic procedures, administer slowly
by intravenous injection. Inject carefully to
avoid deposition outside of the vein. The usual
dose is 30 mg per pound of body weight (15
mL/100 lb). May be repeated at weekly
intervals, if necessary.


Warning



Not for use in lactating dairy cows.


Veterinary Indications



For Animal Use Only


Warnings



Keep Out of Reach Of Children


Caution:



Federal law restricts this drug to use
by or on the order of a licensed veterinarian.


Composition



Each 100 mL of sterile aqueous solution contains:
Sodium Iodide...................20 grams
Water For Injection.................q.s.


Storage And Handling



Store between 15°C-30°C (59°F-86°F).


Warnings And Precautions



TAKE TIME OBSERVE LABEL DIRECTIONS


Information For Owners/Caregivers



Manufactured by:

Nova-Tech, Inc.

Grand Island, NE 68801 USA

18-819

RMS 92-366

NDC# 65207-819-25

Net Contents:

250 mL (8.45 fl oz)

Assembled in USA

Lot No.

Exp. Date


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