Cattle-Mate Injection

Страна: Австралия

Язык: английский

Источник: APVMA (Australian Pesticides and Veterinary Medicines Authority)

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Активный ингредиент:

GONADORELIN AS GONADORELIN ACETATE

Доступна с:

VETOQUINOL AUSTRALIA PTY LTD

Фармацевтическая форма:

PARENTERAL LIQUID/SOLUTION/SUSPENSION

состав:

GONADORELIN AS GONADORELIN ACETATE HORMONE-GONADOTROPHIN Active 100.0 ug/ml

Штук в упаковке:

100mL; 20mL

класс:

VM - Veterinary Medicine

Терапевтические области:

ENDOCRINE SYSTEM

Обзор продуктов:

Poison schedule: 4; Withholding period: Zero (0) days. An ESI has not been esta blished for this product. Note—observin g the meat withholding period may not be sufficient to mitigate potential risks to export trade. Trade advice should be sought from RANDLAB AUSTRALIA PTY LTD on 02 9728 3505 before using this produc t.; Host/pest details: CATTLE - ADULT: [CYSTIC OVARIES, DELAYED OVULATION, IMPROVEMENT OF POSTPARTUM FERTILITY, SYNCHRONISATION OF OESTRUS]

Статус Авторизация:

Registered

Дата Авторизация:

2023-07-01

тонкая брошюра

                                Product Name:
APVMA Approval No:
Cattle-Mate Injection
81105/102328
Label Name:
Cattle-Mate Injection
Signal Headings:
PRESCRIPTION ANIMAL REMEDY
KEEP OUT OF REACH OF CHILDREN
FOR ANIMAL TREATMENT ONLY
Constituent
Statements:
Each ml Cattle Mate Injection contains:
Gonadorelin (as acetate): 100mcg/ml.
Claims:
For use in oestrus synchronization programs in combination with
PGF2α. For the treatment
of cystic ovaries, prevention of delayed ovulation and improvement of
post partum fertility in
cattle.
Net Contents:
20ml and 100ml
Directions for Use:
Restraints:
Contraindications:
Precautions:
Side Effects:
Dosage and
Administration:
Stability studies have demonstrated Cattle-Mate Injection is stable
for 14 days following first
use, providing aseptic technique is followed.
Following withdrawal of the first dose, use the remainder of the vial
within 14 days or
discard the unused portion. RLP APPROVED
Cattle: Injection to be given into the anterior half of the neck.
Cystic ovaries: 5mL (500µg gonadorelin) by intramuscular injection.
Prevention of delayed ovulation: 2.5ml (250µg gonadorelin) by
intramuscular injection.
Improvement of post-partum fertility: 2.5ml (250µg gonadorelin) by
intramuscular injection.
Oestrus Synchronisation: 1ml (100µg gonadorelin) by intramuscular
injection, for example:
Day 0: .......................1ml Cattle Mate Injection
Day 7:........................2ml PGF2α
Day 9: .......................1ml Cattle Mate Injection
Insemination..............8-24 hours after second Cattle Mate
Injection
General Directions:
Withholding Periods:
Zero (0) days.
Trade Advice:
EXPORT SLAUGHTER INTERVAL (ESI): An ESI has not been established for
this product.
Note—observing the meat withholding period may not be sufficient to
mitigate potential
risks to export trade. Trade advice should be sought from RANDLAB
AUSTRALIA PTY LTD
on 02 9728 3505 before using this product.
Safety Directions:
First Aid Instructions:
If poisoning occurs, contact a doctor or Poisons Information Centre.
Phone Australia 13 11
26 N
                                
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Характеристики продукта

                                PRODUCT NAME: CATTLE-MATE GONADORELIN INJECTION
PAGE: 1 OF 5
This revision issued: December, 2017
SAFETY DATA SHEET
Issued by: Randlab Australia Pty Ltd
Phone: (61-2) 9728 3505
POISONS INFORMATION CENTRE: 13 1126 FROM ANYWHERE IN AUSTRALIA, (0800
764 766 IN NEW ZEALAND)
SECTION 1 - IDENTIFICATION OF THE MATERIAL AND SUPPLIER
RANDLAB AUSTRALIA PTY LTD
PHONE: (61-2) 9728 3505
7/85 ALFRED RD
FAX: (61-2) 9728 4352
CHIPPING NORTON, NSW 2170, AUSTRALIA
CHEMICAL NATURE:
Gonadorelin is a synthetic version of gonadotropin-releasing hormone
(GnRH)
TRADE NAME:
CATTLE-MATE GONADORELIN INJECTION
PRODUCT USE:
For use in oestrus synchronisation programs in combination with
PGF2α. For the
treatment of cystic ovaries, prevention of delayed ovulation and
improvement of
postpartum fertility in cattle.
CREATION DATE:
DECEMBER, 2010
THIS VERSION ISSUED:
DECEMBER, 2017
and is valid for 5 years from this date.
POISONS INFORMATION CENTRE: PHONE 13 1126 FROM ANYWHERE IN AUSTRALIA
SECTION 2 - HAZARDS IDENTIFICATION
STATEMENT OF HAZARDOUS NATURE
This product is classified as:
Not classified as hazardous according to the criteria of SWA.
Not a Dangerous Good according to Australian Dangerous Goods (ADG)
Code, IATA and IMDG/IMSBC criteria.
SUSMP CLASSIFICATION:
S4
ADG CLASSIFICATION:
None allocated. Not a Dangerous Good under the ADG Code.
UN NUMBER:
None allocated
GHS SIGNAL WORD: NONE. NOT HAZARDOUS.
PREVENTION
P102: Keep out of reach of children.
P262: Do not get in eyes, on skin, or on clothing.
RESPONSE
P337: If eye irritation persists: seek medical attention.
P353: Rinse skin or shower with water.
P301+P330+P331: IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P370+P378: Not combustible. Use extinguishing media suited to burning
materials.
STORAGE
P410: Protect from sunlight.
P411: Store at temperatures not exceeding 30°C.
DISPOSAL
P501: Dispose of small quantities and empty containers by wrapping
with paper and putting in garbage. For
larger quantities, if recycling or reclaiming is not possible, use a
commercial waste disposal s
                                
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