Product information

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No other product was found with the same active ingredient group.

The product monograph is developed by a drug sponsor according to guidelines published by Health Canada that provide direction on the content and format. The veterinary labelling is developed by the drug sponsor according to the Food and Drug Regulations. While Health Canada reviews the product monograph or the veterinary labelling as part of the drug review process, it remains the responsibility of the drug sponsor to ensure that the product monograph or the veterinary labelling is complete and accurate.

Current status:

Cancelled Post Market

Current status date:

2018-06-28

Original market date: ^{See footnote 1}

1993-12-31

Lot number: ^{See footnote 2}

W6J19C3

Expiry date: ^{See footnote 2}

2017-10-31

Product name:

CLINIMIX E

Description:

4.25 % AMINO ACIDS (BLEND B) WITH ELECTROLYTES IN 10% DEXTROSE INJECTION

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DIN:

02014025

Product Monograph/Veterinary Labelling:

Date: 2015-04-30 Product monograph/Veterinary Labelling (PDF version ~ 175K)

Company:

BAXTER CORPORATION
7125 Mississauga Road
Mississauga
Ontario
Canada L5N 0C2

Class:

Human

Dosage form(s):

Solution

Route(s) of administration:

Intravenous

Number of active ingredient(s):

Schedule(s):

Ethical

American Hospital Formulary Service (AHFS): ^{See footnote 3}

40:12.00 , 40:20.00

Anatomical Therapeutic Chemical (ATC): ^{See footnote 4}

B05BA10 COMBINATIONS

Active ingredient group (AIG) number:^{See footnote5}

1950854024

List of active ingredient(s)
Active ingredient(s)	Strength
DEXTROSE	10 G / 100 ML
GLYCINE	880 MG / 100 ML
HISTIDINE	186 MG / 100 ML
L-ALANINE	880 MG / 100 ML
L-ARGININE	440 MG / 100 ML
L-ISOLEUCINE	203 MG / 100 ML
L-LEUCINE HYDROCHLORIDE	263 MG / 100 ML
L-LYSINE HYDROCHLORIDE	246 MG / 100 ML
L-PHENYLALANINE HYDROCHLORIDE	263 MG / 100 ML
L-PROLINE	178 MG / 100 ML
L-THREONINE	178 MG / 100 ML
L-TYROSINE	17 MG / 100 ML
L-VALINE	195 MG / 100 ML
MAGNESIUM CHLORIDE	51 MG / 100 ML
METHIONINE	246 MG / 100 ML
POTASSIUM PHOSPHATE DIBASIC	261 MG / 100 ML
SODIUM ACETATE	297 MG / 100 ML
SODIUM CHLORIDE	77 MG / 100 ML
TRYPTOPHAN	76 MG / 100 ML

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Footnotes

Footnote 1

The earliest marketed date recorded in the Drug Product Database.

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Footnote 2

When a manufacturer decides to discontinue the sale of their drug, the date of discontinuation is the date of the last sale by the manufacturer. The DIN will be cancelled further to the receipt of a sale discontinuation notification from the manufacturer. The status of the DIN will be updated to “Cancelled (Post-Market)” in the online Drug Product Database. For DINs cancelled on or after March 14, 2017, the latest expiry date and lot number of the product distributed in Canada will be posted on the online Drug Product Database. Other parties in the health product distribution chain such as wholesalers, retailers, pharmacists and medical practitioners may still sell or distribute that drug after DIN cancellation if the expiry date of the drug lot has not passed. This may be acceptable so long as the DIN cancellation is not due to health and/or safety reasons.

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Footnote 3

The American Hospital Formulary Service permits an easy review of information on a group of drugs with similar activities and uses and allows the reader to determine quickly the similarities and differences among drugs within a group. AHFS® Pharmacologic/Therapeutic Classification© used with permission. © 2022, the American Society of Health-System Pharmacists, Inc. (ASHP). The Data is a part of the AHFS Drug Information®; ASHP is not responsible for the accuracy of transpositions from the original context.

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Footnote 4

The purpose of the World Health Organization (WHO) Anatomical Therapeutic Chemical (ATC) classification system is to be used as a tool for drug utilization research in order to improve quality of drug use. Drugs are divided into different groups according to the organ or system on which they act and their chemical, pharmacological and therapeutical properties.

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Footnote 5

The AIG number is a 10 digit number that identifies products that have the same active ingredient(s) and ingredient strength(s). The AIG is comprised of three portions:

the first portion (2 digits) identifies the number of active ingredients,
the second portion (5 digits) identifies the unique groups of active ingredients(s),
the last portion (3 digits) identifies the active ingredient group strength. The strength group has a tolerance of ‑2% to +10%.

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Date modified:: 2019-03-01