CMPK injection, solution

CMPK by

Drug Labeling and Warnings

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

Drug Details [pdf]

Each 500 mL Contains

Dextrose  H2O.................................... 75.0 g

Calcium .............................................. 10.8 g

(as calcium borogluconate)

Potassium  ...........................................  8.0 g

(as potassium chloride)

Phosphorus  .......................................... 2.5 g

(as sodium hypophosphite H2O)

Magnesium ........................................... 1.6 g

(as magnesium borogluconate)

INDICATIONS

For use in cattle as an aid in treatment of conditions associated with calcium,
magnesium, phosphorus, potassium or glucose deficiencies.

CONTRAINDICATIONS

DO NOT administer this product to animals showing signs of cardiac distress. Monitor animal's condition closely.

CAUTION

Entire contents should be used when first entered as this product contains no preservatives. Do not use if solution is not clear.
Discard any unused portion.

DOSAGE & ADMINISTRATION:

Cattle ...............500 mL/800-1000 lbs body weight.

For intravenous administration only. Solution should be warmed to body temperature and administered slowly using aseptic precautions.

STORAGE AND HANDLING

Store between 15°C - 30°C (59°F - 86°F).

WARNINGS AND PRECAUTIONS

TAKE TIME OBSERVE LABEL DIRECTIONS

Keep Out of Reach of Children

VETERINARY INDICATIONS

For Animal Use Only

CAUTION:

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

INFORMATION FOR OWNERS/CAREGIVERS

Manufactured by:

Nova-Tech, Inc.

Grand Island, NE 68801 USA

18-805

RMS 92-336

NDC: 65207-805-50

Nova-Tech® Animal Health

Calcium-Magnesium-Phosphorus-Potassium-Dextrose

Steril Solution

Net Contents:

500 mL (16.91 fl oz)

Assembled in USA

Lot No. 

Exp. Date

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CMPK 
cmpk injection, solution

Product Information
Product Type	PRESCRIPTION ANIMAL DRUG	Item Code (Source)	NDC: 65207-805
Route of Administration	INTRAVENOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Dextrose monohydrate (UNII: LX22YL083G) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)	Dextrose monohydrate	75.0 g  in 500 mL
Potassium Chloride (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CATION	8.0 g  in 500 mL
Calcium Gluconate Monohydrate (UNII: CZN0MI5R31) (CALCIUM CATION - UNII:2M83C4R6ZB)	Calcium Gluconate Monohydrate	10.8 g  in 500 mL
Phosphorus (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W)	Phosphorus	2.5 g  in 500 mL
Magnesium Gluconate (UNII: T42NAD2KHC) (MAGNESIUM CATION - UNII:T6V3LHY838)	Magnesium Gluconate	1.6 g  in 500 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65207-805-50	500 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/18/2020

Labeler - Nova-Tech, Inc. (196078976)

Registrant - Nova-Tech, Inc. (196078976)

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