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Cloprostenol Sodium Injection

Cloprostenol Sodium Injection

Cloprostenol Sodium Injection is a synthetic prostaglandin F2α analogue widely used in veterinary reproductive management. This powerful luteolytic agent effectively regulates estrous cycles in cattle and induces parturition in swine, making it an essential tool for modern livestock breeding programs. As a potent uterotonic medication, it stimulates uterine contractions while causing corpus luteum regression, enabling precise control of reproductive timing in farm animals.

Product Introduction

 

Cloprostenol Sodium Injection

Veterinary Drug

Veterinary Drug Name

 

Generic Name: Cloprostenol Sodium Injection

Main Ingredient

 

Cloprostenol Sodium

Description / Appearance

 

This product is a colorless, clear liquid.

Pharmacological Action

 

Cloprostenol Sodium is a synthetic analogue of prostaglandin F2α with the following effects:

Luteolytic effect: Rapid regression of the corpus luteum and inhibition of its secretion.

Uterotonic effect: Direct stimulation of uterine smooth muscle, causing uterine contractions and cervical relaxation.

Effects on Animals

In animals with normal estrous cycles: estrus usually occurs within 2–5 days after administration.

In pregnant cows at 10–150 days gestation: abortion usually occurs 2–3 days after injection.

Indications and Usage

 

Prostaglandins have a strong luteolytic effect and directly stimulate uterine smooth muscle. They are mainly used for estrus synchronization in cows and induction of parturition in pregnant sows.

Dosage and Administration

 

Intramuscular (IM) Injection

 

▸ Cattle: 2–3 ml per dose.

▸ Pigs: 0.5–1 ml on day 112–113 of pregnancy.

Adverse Reactions

 

Use during late pregnancy may increase the risk of dystocia (difficult birth) and may result in decreased efficacy.

Precautions

 

1. Contraindication: Do not use in pregnant animals unless intended for induction of parturition or termination of pregnancy.

2. Induction of Farrowing: Use no earlier than 2 days before the expected farrowing date.

3. Human Safety: This product can induce abortion or acute bronchospasm in humans. Pregnant women, women of childbearing age, asthmatics, and persons with respiratory diseases must exercise extreme caution.

4. Accidental Exposure: If breathing difficulties occur due to accidental inhalation or injection, use a fast-acting bronchodilator and seek medical attention.

5. Dermal Absorption: Easily absorbed through the skin. Wear rubber or disposable gloves during handling. Wash hands thoroughly with soap and water after use and before eating/drinking. Flush skin immediately with clear water if contact occurs.

6. Drug Interactions: Do not use concurrently with non-steroidal anti-inflammatory drugs (NSAIDs).

7. Disposal: Empty vials should be deeply buried or incinerated. Dispose of waste in approved facilities. Do not dispose of undiluted product on-site. Prevent contamination of water, feed, and food.

Withdrawal Period

 

None required.

Storage

 

Store in a sealed, cool and dark place.

Product Information

 

Strength

 

 2 ml:0.2 mg

5 ml : 0.5 mg

20 ml: 2 mg

 

Packaging

 

10 vials per box

Shelf Life

 

2 years

Approval Number

 

Veterinary Drug Approval No. 130322207

Manufacturer Information

 

Xiamen Origin Biotech Co., Ltd.

 

Address

No. 9-5 Xianghai 2nd Road, Xiang'an Torch High-Tech Industrial Development Zone, Xiamen, Fujian, China.

Postal Code

361101

Telephone

+86-592-7073986

 

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