DEXTROSE- dextrose injection, solution 
Vedco

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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DEXTROSE 50% SOLUTION

DEXTROSE- dextrose injection, solution


Vedco


Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA.

DEXTROSE 50% SOLUTION

KEEP OUT OF REACH OF CHILDREN

ACTIVE INGREDIENTS:

Each 100 mL contains:

Dextrose . H2O .......................... 50 gms.

DOSAGE AND ADMINISTRATION:

For intravenous administration only.


Cattle: 100 to 500 mL depending on size and condition.


Treatment may be repeated in several hours or on successive days as needed. 

STORAGE

Store at 15 degrees C to 30 degrees C (59 degrees F-86 degrees F).

INDICATIONS:

For use as an aid in the treatment of acetonemia (Ketosis) in cattle.

CAUTION:

Intravenous administration must be done slowly and made under strict asepsis. Solution should be warmed to body temperature prior to administration.

This is a single dose container. This product contains no preservative. After a quantity has been withdrawn for injection, the remainder should be discarded. Do not administer intraperitoneally. 

FOR ANIMAL USE ONLY

TAKE TIME OBSERVE LABEL DIRECTIONS

Distributed By
VEDCO, INC.
St. Joseph, MO 64507

Made in El Salvador

TABLE  
 CONTENTS    NDC VINV #
 500 mL 50989-880-16 VINV-DEXT-ROUN

PRINCIPAL DISPLAY PANEL

NDC50989-880-16

ULTIGIENE TERMINALLY STERILIZED

DEXTROSE 50% SOLUTIONS

NET CONTENTS: 500 mL

VEDCO

FOR ANIMAL USE ONLY

KEEP OUT OF REACH OF CHILDREN

Label

DEXTROSE 
dextrose injection, solution
Product Information
Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:50989-880
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK) DEXTROSE MONOHYDRATE50 g  in 100 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50989-880-16500 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other01/09/2019
Labeler - Vedco (021634266)
Registrant - Vedco (021634266)

Revised: 5/2019
Document Id: a3ff75c2-1521-4381-994c-9ff401cefb77
Set id: 3f9d4842-6803-40f7-b233-109f664a48f9
Version: 3
Effective Time: 20190501
 
Vedco