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Ivermectin injection 1% solution

Ivermectin Injection 1%

CAS No.
(Active ingredient – Ivermectin) 70288-86-7
Appearance
Clear to light yellow sterile solution

Purity

1% (w/v) Ivermectin (10 mg/mL)

Molecular Formula

None

Molecular Weight

None

Solubility

Soluble in propylene glycol, ethanol, and vegetable oils; insoluble in water.

Synonyms

Ivermectin injectable solution; Ivermectin 1% sterile injection
A sterile oil-based injectable solution containing 10 mg ivermectin per mL. Broad-spectrum control of internal and external parasites in cattle, sheep, pigs, and camels. Ensures long-lasting protection and safety with a single subcutaneous dose.

Table of Contents

Overview

Ivermectin Injection 1% is a sterile, ready-to-use antiparasitic solution formulated for veterinary use. Each milliliter contains 10 mg ivermectin in a propylene glycol and vegetable oil base, providing consistent absorption and sustained efficacy.

It offers broad-spectrum protection against internal and external parasites in livestock, ensuring long-term health improvement and productivity with a single subcutaneous dose. Suitable for cattle, sheep, pigs, and camels.

Product Information

Composition

  • Each mL contains 10 mg Ivermectin as active ingredient.
  • Vehicle: Propylene glycol, glycerol formal, and vegetable oil.
  • Sterilized by filtration and filled under aseptic conditions.

Pharmacological Action

Ivermectin acts on parasites by increasing chloride ion influx through glutamate-gated channels, leading to paralysis and death. It is effective against nematodes, lice, and mites, with a wide safety margin for treated animals when used as directed.

Technical Specifications

Item Specification
Active Ingredient Ivermectin 10 mg/mL
Appearance Clear or pale yellow sterile solution
Vehicle System Propylene glycol, glycerol formal, vegetable oil
Assay Range 95% – 105%
pH Range 5.0 – 7.0
Sterility Complies with USP/EP standards
Residual Solvents Within limits as per GMP

All analytical data verified in HOPE BIOTECH GMP-certified laboratories in accordance with veterinary pharmacopoeia specifications.

Quality Assurance

Every batch of Ivermectin Injection 1% is manufactured in GMP-compliant facilities under ISO 9001 and ISO 14001 quality systems. Each lot is validated for sterility, potency, and stability before release.

  • Produced under sterile GMP conditions.
  • COA, MSDS, and batch documentation supplied with each shipment.
  • Packaging: 50 mL, 100 mL, and 500 mL amber glass bottles with aluminum caps.

Storage: Store below 30°C, protected from light.
Shelf Life: 24 months from date of manufacture under recommended conditions.

Applications & Dosage

Indicated for the treatment and control of gastrointestinal and pulmonary nematodes, lice, and mange mites in cattle, sheep, pigs, and camels. Administer subcutaneously according to the recommended dosage schedule.

Recommended Dosage

  • Cattle and camels: 1 mL per 50 kg body weight (200 µg/kg)
  • Sheep and goats: 0.5 mL per 25 kg body weight (200 µg/kg)
  • Pigs: 1 mL per 33 kg body weight (300 µg/kg)

Inject subcutaneously in the neck or shoulder area. Do not exceed 10 mL per injection site. Repeat treatment only as advised by a veterinarian.

Product FAQ

Q1: What parasites does Ivermectin Injection 1% control?
A: It controls gastrointestinal roundworms, lungworms, lice, ticks, and mange mites in cattle, sheep, pigs, and camels.

Q2: How does Ivermectin work?
A: It interferes with parasite nerve transmission through glutamate-gated chloride channels, leading to paralysis and death without affecting mammals.

Q3: What is the withdrawal period?
A: 35 days for cattle and sheep; 28 days for pigs. Not for use in lactating animals producing milk for human consumption.

Q4: Can it be used during pregnancy or lactation?
A: Safe at normal therapeutic doses. Avoid high doses during late pregnancy unless directed by a veterinarian.

Q5: What precautions should be taken during administration?
A: Use only sterile equipment and inject under clean, dry skin. Do not mix with other veterinary drugs in the same syringe.

Q6: What are the environmental precautions?
A: Ivermectin is toxic to aquatic life. Dispose of unused or expired product according to local environmental and veterinary waste regulations.

Q1. How can I request a quotation or sample?

You can click the “Send Inquiry” button on this page or email us directly at [email protected].

Samples are available for most products, and our sales team will reply within 24 hours with detailed pricing and documentation .

Q2. What is the minimum order quantity (MOQ)?

The MOQ is 0.5 kg for most products.

For laboratory evaluation or small trial batches, smaller quantities can be arranged depending on stock availability.

Q3. What certifications do your products comply with?

Our GMP-certified partners operate under ISO, CEP, and FSC standards.

Each batch is supplied with a full set of COA, MSDS, and export documents to ensure quality traceability.

Q4. How long does delivery take?

Usually 3–7 working days for available stock and 2–3 weeks for customized specifications or large orders.

Q5. Which payment methods do you accept?

We accept T/T, L/C, and other agreed terms depending on the order volume and region.

Q6. Can you provide contract manufacturing or custom formulation support?

Yes. We cooperate with multiple GMP facilities to offer custom synthesis, formulation, and registration support for specific markets.

Packaging Information

  • Standard packing: 25 kg fiber drum or 1 kg foil bag

  • Double PE inner liner for moisture protection

  • Custom packaging available on request

Storage & Stability

Store in a cool, dry environment away from direct light. Shelf life 24 months under recommended conditions.

Transportation

Shipped by air, sea, or express according to customer preference. Dangerous goods comply with IATA/IMDG standards if applicable.

Company Certifications
Company quality and compliance certificates

Our company and partner facilities hold valid GMP and ISO certificates issued by national authorities, ensuring that every batch meets strict quality and traceability standards required for international veterinary API markets.

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