DEXTROSE 50% SOLUTION- dextrose injection, solution

Dextrose 50% Solution by

Drug Labeling and Warnings

Dextrose 50% Solution by is a Animal medication manufactured, distributed, or labeled by Nova-Tech, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Dosage And Administration:

The usual dose is 50 mL per 100 lbs of body weight. It should be administered intravenously only. Dosage may be repeated in 8 to 10 hours or on successive days if necessary.

Caution:

It should be warmed to body temperature and administered slowly. This product contains no presevatives. Do not use if solution is not clear. Entire contents should be used upon opening. Discard any unused portion.

GENERAL PRECAUTIONS

FOR ANIMAL USE ONLY
KEEP OUT OF REACH OF CHILDREN

Active Ingredients

Dextrose H2O...........................50% w/v

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

Indications:

Dextrose 50% Solution is indicated for use as an aid in the treatment of uncomplicated primary ketosis in cattle.

STORAGE AND HANDLING

Store between 15°C-30°C (59°F-86°F).

GENERAL PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

INFORMATION FOR OWNERS/CAREGIVERS

Manufactured by:

Nova-Tech, Inc.

Grand Island, NE 68801 USA

18-801

RMS 92-325

NDC# 65207-801-50

Nova-Tech® Animal Health

Dextrose 50% Solution

Sterile Solution

Net Contents:

500 mL (16.91 fl oz)

Assembled in USA

Lot No.               Exp. Date

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DEXTROSE 50% SOLUTION 
dextrose injection, solution

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 65207-801
Route of Administration	INTRAVENOUS

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: 65207-801-50	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/13/2020

Labeler - Nova-Tech, Inc. (196078976)

Registrant - Nova-Tech, Inc. (196078976)

Establishment
Name	Address	ID/FEI	Business Operations
Nova-Tech, Inc.		196078976	manufacture, api manufacture