DEXTROSE injection, solution

Dextrose by

Drug Labeling and Warnings

Dextrose by is a Animal medication manufactured, distributed, or labeled by Durvet. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & 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.

CAUTIONS

Intravenous administration must be done slowly and made under stric 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 After a quantity has been withdrawn for injection, the remainder should be discarded.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

ACTIVE INGREDIENTS:

Each 100 mL contains:

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

STORAGE AND HANDLING

Store between 15°C and 30°C (59°F and 86°F)

INDICATIONS:

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

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

VETERINARY INDICATIONS

FOR USE IN ANIMALS ONLY

SAFE HANDLING WARNING

TAKE TIME. OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

REV 06-19

ISS19XB04

Manufactured for:

​DURVET, INC.​

Blue Springs, Missouri 64014

www.durvet.com

Principal Display Panel

NDC: 30798-127-17

durvet

DEXTROSE 50% SOLUTION

Dura-Ster TS

TERMINALLY STERILIZED

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

​NET CONTENTS: 500 mL

(16.9 fl. oz.)

INGREDIENTS AND APPEARANCE

DEXTROSE 
dextrose injection, solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 30798-127
Route of Administration	INTRAVENOUS, INTRAMUSCULAR, INTRAPERITONEAL, SUBCUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROSE MONOHYDRATE (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)	DEXTROSE MONOHYDRATE	50 g  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 30798-127-17	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/07/2019

Labeler - Durvet (056387798)

Registrant - Durvet (056387798)