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Tylvalosin tartrate (CAS 63428-13-7) premix 50% for veterinary use

Tylvalosin Tartrate Premix 50%

CAS No.
None
Appearance
Yellow-brown to light brown powder

Purity

Formulated concentration: 50% w/w

Molecular Formula

None

Molecular Weight

None

Solubility

Practically insoluble in water; uniform dispersion in feed carriers

Synonyms

Tylvamycin Tartrate Premix 50%, High Concentration Tylvalosin Feed Premix
High-concentration feed premix containing 50% Tylvalosin Tartrate, formulated for efficient control of mycoplasma and bacterial respiratory diseases in pigs and poultry.

Table of Contents

Overview


Tylvalosin Tartrate Premix 50% is a high-strength veterinary feed formulation containing 50% of the macrolide antibiotic Tylvalosin Tartrate. It is used for the treatment and prevention of respiratory and enteric infections caused by Mycoplasma, Pasteurella, and Gram-positive bacteria in pigs and poultry.

This formulation is designed for professional feed mills and veterinary drug manufacturers that require precise dosage control and smaller inclusion rates. It ensures excellent bioavailability, uniform dispersion, and cost efficiency for mass feed production.

Unlike the 20% premix, this product delivers higher potency with reduced inclusion volume, improving feed formulation flexibility while maintaining therapeutic efficacy.

Product Information


Product Name Tylvalosin Tartrate Premix 50%
Active Ingredient Tylvalosin Tartrate – 50% w/w
Product Grade Feed Grade (Veterinary Use Only)
Appearance Yellow-brown or light brown powder
Mode of Action Inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit, effectively controlling Mycoplasma and Gram-positive bacterial infections.
Target Species Pigs and Poultry
Main Benefits • High concentration reduces feed volume usage
• Fast onset of action and superior efficacy
• Improves growth performance and reduces mortality
Packaging 25 kg per bag / drum or as customized
Storage Store in a cool, dry, and well-ventilated place below 25°C.
Shelf Life 24 months under recommended storage conditions

Technical Specifications


Formulation Type Premix (High Concentration)
Concentration 50% w/w Tylvalosin Tartrate
Carrier Feed-grade excipients with high dispersibility
Moisture Content ≤5.0%
Loss on Drying ≤6.0%
Microbial Limits Complies with veterinary feed additive standards
Manufacturing Standard Produced in GMP-certified veterinary feed facilities
Export Documentation COA, MSDS, Veterinary Certificate, Certificate of Origin, CIQ (if required)

Quality Assurance


Every batch of Tylvalosin Tartrate Premix 50% produced by HOPE BIOTECH follows stringent quality control procedures to guarantee product safety and efficacy.

  • Manufactured under ISO 9001 and GMP feed additive standards.
  • Each lot is tested for active content, homogeneity, and microbial safety.
  • COA and batch sample retention for full traceability.
  • Quality documentation includes COA, MSDS, and Veterinary Health Certificate for export compliance.

Applications & Dosage


  • Indications: For the prevention and treatment of Mycoplasma infections, chronic respiratory disease, and secondary bacterial infections in pigs and poultry.
  • Pigs: 100–150 g of product per 1000 kg of feed for 7 days.
  • Chickens: 200–600 g of product per 1000 kg of feed for 7 days.
  • Withdrawal Period: 3 days for pigs, 5 days for chickens.
  • Usage: Mix thoroughly with feed to ensure homogeneous distribution. Not for direct oral administration or injection use.
  • Compatibility: Avoid concurrent use with other macrolides or β-lactam antibiotics (e.g., penicillin).

Product FAQ


Q1: What distinguishes Tylvalosin Tartrate Premix 50% from the 20% version?
A1: The 50% version offers double concentration, reducing feed inclusion rates by up to 60%. It is designed for industrial feed mills requiring high efficiency and smaller formulation volumes.

Q2: Is it suitable for direct use in farms?
A2: It can be used on large-scale farms with proper feed mixing equipment, but it is primarily intended for professional premix and veterinary formulation manufacturers.

Q3: What is the withdrawal period for meat products?
A3: 3 days for pigs and 5 days for chickens, ensuring residue-free compliance for export markets.

Q4: What documentation can HOPE BIOTECH provide?
A4: We supply COA, MSDS, Veterinary Certificate, and CIQ inspection reports upon request.

Q5: Can it be mixed with other antibiotic premixes?
A5: Co-administration with macrolides or penicillin is not recommended due to possible antagonistic effects.

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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