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Tylvalosin Tartrate Premix 20%
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Overview
Tylvalosin Tartrate Premix 20% is a feed-grade veterinary formulation containing 20% of the macrolide antibiotic Tylvalosin Tartrate. It is used for the prevention and treatment of mycoplasma infections and related respiratory diseases in pigs and poultry. The product is manufactured in GMP-certified feed additive facilities and designed for easy inclusion in feed mills or on-farm mixing.
Unlike the pharmaceutical-grade API, this premix is ready to use in feed formulations and does not require further processing. It offers consistent particle size, excellent uniformity, and high bioavailability, ensuring reliable therapeutic outcomes while minimizing antibiotic residues in livestock products.
Product Information
| Product Name | Tylvalosin Tartrate Premix 20% |
| Active Ingredient | Tylvalosin Tartrate – 20% w/w |
| Product Grade | Feed Grade (Veterinary Use Only) |
| Appearance | Light yellow or brownish-yellow powder |
| Mode of Action | Inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit, effectively controlling Mycoplasma and Gram-positive pathogens. |
| Target Species | Pigs, Broilers, Layers |
| Main Benefits | Excellent efficacy against Mycoplasma hyopneumoniae and Mycoplasma gallisepticum; improves growth performance and feed conversion. |
| Packaging | 25 kg per bag / drum or customized |
| Storage | Store in a cool, dry place below 25°C. Protect from moisture and direct sunlight. |
| Shelf Life | 24 months when stored properly |
Technical Specifications
| Formulation Type | Premix |
| Concentration | 20% w/w Tylvalosin Tartrate |
| Carrier | Selected feed-grade excipients ensuring homogeneous distribution |
| Moisture Content | ≤5.0% |
| Loss on Drying | ≤6.0% |
| Microbial Limits | Conforms to feed additive quality standards |
| Manufacturing Standard | Produced in GMP-certified veterinary feed additive facilities |
| Export Documents | COA, MSDS, Veterinary Certificate, Certificate of Origin, CIQ if required |
Quality Assurance
HOPE BIOTECH ensures that every batch of Tylvalosin Tartrate Premix 20% meets international feed additive standards. The product is manufactured in facilities implementing ISO 9001 and GMP feed production systems, with complete traceability and documentation.
- Each lot undergoes rigorous testing for assay, uniformity, and microbial limits.
- Full documentation provided: COA, MSDS, and Veterinary Health Certificate.
- Batch samples are retained for 2 years for post-market verification.
- Packaging and labeling follow FAO/WHO feed additive guidelines.
Applications & Dosage
- Indications: For prevention and treatment of mycoplasma infections, chronic respiratory disease, and bacterial enteritis in pigs and poultry.
- Pigs: 250–375 g of product per 1000 kg of feed for 7 days.
- Chickens: 500–1500 g of product per 1000 kg of feed for 7 days.
- Withdrawal Period: 3 days for pigs, 5 days for chickens.
- Compatibility: Should not be used concurrently with penicillin or other macrolide antibiotics.
- Usage: Mix thoroughly with feed to ensure uniform distribution. Not intended for direct oral administration or pharmaceutical processing.
Product FAQ
Q1: What is the main difference between Tylvalosin Tartrate Premix 20% and the API?
A1: The API is a raw material (≥98% purity) used for pharmaceutical manufacturing, while the 20% premix is a ready-to-use feed additive formulated for direct inclusion in animal feed.
Q2: Can it be used together with other antibiotics?
A2: It should not be used in combination with penicillin or other macrolides to avoid antagonistic effects.
Q3: What animals benefit most from this product?
A3: It is most effective for pigs and chickens affected by Mycoplasma infections and respiratory disease complexes.
Q4: What quality certifications are available?
A4: HOPE BIOTECH’s premix series are produced under ISO 9001 and GMP-certified systems with full COA and Veterinary Certificates available for export.
Q5: What are the storage and stability conditions?
A5: Store below 25°C in a cool, dry place, protected from moisture and light. Shelf life is 24 months under proper conditions.
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.
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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