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HS Code |
420159 |
| Product Name | Pyrantel Pamoate Tablets Veterinary Grade API |
| Appearance | Yellow to light brown powder |
| Chemical Formula | C11H14N2S · C23H16O6 |
| Molecular Weight | 594.7 g/mol |
| Solubility | Practically insoluble in water, slightly soluble in alcohol |
| Purity | ≥98% (by HPLC) |
| Intended Use | Anthelmintic for veterinary use |
| Dosage Forms | Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions |
| Storage Conditions | Store below 25°C, protected from light and moisture |
| Mechanism Of Action | Depolarizing neuromuscular blocking agent causing paralysis of helminths |
As an accredited Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed HDPE bottle containing 500g Pyrantel Pamoate Veterinary Grade API, labeled with batch, purity, usage, precautions, and manufacturer details. |
| Shipping | The shipping of Pyrantel Pamoate Tablets (Veterinary Grade API) is conducted in compliance with international safety standards, packaged in moisture-proof, tamper-evident containers. Products are securely boxed, labeled according to regulatory requirements, and shipped via reliable, temperature-controlled logistics to ensure product integrity during transit. Customized packaging options are available upon request. |
| Storage | Store Pyrantel Pamoate Tablets (Veterinary Grade API) in a tightly sealed container, protected from light, moisture, and excessive heat. Maintain storage at a cool, dry place, ideally below 25°C (77°F). Keep away from incompatible substances and ensure proper ventilation. Store out of reach of children, unauthorized personnel, and animals. Follow local regulations for chemical storage and handling. |
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Purity 98%: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with 98% purity is used in mass deworming programs for livestock, where it ensures rapid and effective parasite elimination with minimal residue. Particle Size D90 < 10 µm: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size D90 less than 10 microns is used in oral suspension formulations, where it achieves enhanced bioavailability and uniform dispersion in solution. Melting Point 155°C: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with a melting point of 155°C is used in the manufacturing of heat-stable veterinary boluses, where it maintains chemical integrity during thermal processing. Stability Temperature up to 45°C: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with stability up to 45°C is used in tropical field supply chains, where it prevents degradation and assures product efficacy during transportation and storage in elevated ambient temperatures. Moisture Content <1%: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with moisture content below 1% is used in water-soluble powder mixes, where it reduces the risk of clumping and ensures precise dosing. Pharmacopoeial Grade: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with pharmacopoeial compliance is used in regulated veterinary pharmaceutical manufacturing, where it guarantees safety and meets international veterinary standards. Solubility in Water: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with enhanced water solubility is used in injectable antiparasitic solutions, where it results in faster onset of therapeutic action. Residual Solvent < 0.05%: Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with residual solvent levels below 0.05% is used in high-purity injectable formulations, where it minimizes toxicity risks and complies with global veterinary drug regulations. |
Competitive Pyrantel Pamoate Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions prices that fit your budget—flexible terms and customized quotes for every order.
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Our experience manufacturing Pyrantel Pamoate Tablets spans decades in the veterinary field. This active pharmaceutical ingredient (API) has proven its worth in controlling gastrointestinal parasites in a wide range of animal species. In our production lines, we prioritize batch consistency and careful monitoring of every lot, knowing that animal health professionals count on us to provide effective, safe, and straightforward solutions that will work in dogs, cats, livestock, and companion animals. Pyrantel Pamoate stands apart thanks to the reliability it offers for integrated parasite management in either tablet, injection, capsule, powder, granule, premix, or solution forms.
Pyrantel Pamoate's chemical stability is crucial for manufacturers developing dosage forms suited to field conditions. Over countless batches, we have maintained the strictest purity standards with a model focused on minimizing residual solvents and impurities, so veterinarians and producers benefit from the full pharmacological action of pyrantel against nematodes like Toxocara and Ancylostoma. Our premium-grade API enables predictable formulations whether blended into feed premix, compressed as single-dose tablets, or dissolved in oral solutions. Reliability does not happen by chance. Our process draws on twelve years of continuous process improvement, attention to granulation parameters, and collaboration with formulation scientists who want APIs that behave the same, every time.
Our Pyrantel Pamoate powder flows easily, avoiding the clumping that can disrupt tablet compression or precise dosing. This makes the API suitable for high-speed tableting and capsule filling–protecting throughput and finished product quality. For injectables, the grade we supply dissolves in standard vehicle solutions with no unusual residue or discoloration, which matters when clarity and solubility are critical for regulatory batch release and field use. Blending into premix or granule products for on-farm application brings its own hurdles: particle size and density must permit homogeneous distribution in feed, and our repeated investment into new milling equipment pays off when large-scale feed manufacturers smoothly introduce the API into production lines without waste or dust problems.
Oral suspensions or solutions made for small animals demand not only precise dosing but also good mouthfeel and stability, especially at a range of storage temperatures. Manufactured consistently, our product has enabled contract partners to reduce their recalls and field complaints linked to precipitation or flavor problems, thanks to improved carrier binding and minimal bitterness.
For years, gastrointestinal worms have plagued livestock and pet animals worldwide, affecting growth rates, fertility, wool quality, and even the safety of animal-derived food. Pyrantel, as a tetrahydropyrimidine derivative, works as a nicotinic receptor agonist–leading to quick paralysis and expulsion of susceptible nematodes. Unlike benzimidazoles and macrocyclic lactones, it does not linger in the tissue. Residue periods remain short, which matters to food producers aiming to meet regulatory guidelines and assure buyers. From direct experience, farm veterinarians and horse owners repeat treatments regularly, switching from oral pastes to tablets for more flexible dosing in young animals, or using premixed feed when treating large herds.
This product's value increases where parasite resistance to other drug classes rises. Some classes of endoparasiticides no longer perform as reliably, but Pyrantel Pamoate, used responsibly, continues to help veterinarians break the re-infection cycle, especially in areas where livestock production intensity drives worm burdens higher. Our direct relationships with farming cooperatives and animal clinics keep us updated on field trends so we optimize for the needs not of a theoretical customer, but of people running active barns, feedlots, or clinics.
Standing in the factory, it’s easy to treat bulk powder as a generic item. In reality, minor upstream process differences produce batches that look similar but behave differently in final formulations. Some large-scale producers in the region focus on low-cost input and maximize volume, but our team saw how this approach led to batch failures, poor solubility, and customer complaints. Direct customer feedback made us double down on particle engineering and careful solvent handling. Where others cut corners on process time or blending to chase short-term sales, we’ve seen far better long-term loyalty come from refusing to ship if tests fall outside a tight standard curve.
Formulators distinguish between products based on reactivity, stability, and how they perform in multiple finished dosage forms. Competing products often rely on coarser particle sizes, unoptimized polymorph blends, or less precise moisture control, impacting the end user. In field trials with local tablet manufacturers, our batch passed dissolution and friability standards more often under stress conditions. For veterinarians, this translates to a lower rate of physical or chemical failure in tablets or suspensions during shipping and storage.
We do not sell blends mixed with calcium carbonate or other bulking agents. Feedback from global partners highlighted problems blending off-standard bulk powders, particularly for new animal products targeting horses, dogs, and goats—where taste and performance must be tightly managed. With direct-from-source production, the risk of cross-contamination or adulteration in the supply chain drops sharply. Transparency and traceability ensure we can verify raw material sources and batch analytics when our customers audit the site. That allows us to maintain long-term registrations and supply agreements with regulated pharmaceutical companies, supplement makers, and private-label feed mills.
Years spent working as a manufacturer in this sector have taught us quality cannot rely solely on documentation or external certification. Site inspections conducted by customers and regulators alike drive constant improvement. We have responded to site observations by altering filtration steps, recalibrating combinational blending tanks, and improving climate control inside production blocks handling Pyrantel Pamoate. These investments make a difference not only in numbers on a test result, but also on how product travels across countries, and ultimately, whether it works as planned for a veterinarian treating a valuable dairy herd or foal.
Recovery rates, impurity levels, heavy metal testing, and residual solvent measurements have become more stringent in recent years. Our records show consistent compliance with both local and foreign pharmacopeias, including repeated acceptance into regulated markets. We maintain comprehensive batch histories and raw data required during international inspections. Animal health regulators now expect full origin tracing not only for our main product but also for minor excipients and process chemicals. Our team works constantly to guarantee every shipment can be tracked back to original synthetic steps and source chemicals.
At times, we have refused short-notice “spot demand” orders when they might have forced us to cut corners or deviate from protocol. That choice sacrificed sales but protected trust. Repeat buyers have told us that maintaining audit readiness, clear Certificate of Analysis reporting, and unbroken cold chain delivery meant more than a discounted invoice.
Long-term success comes from improved field outcomes, not just certifications or sales data. One mid-sized poultry cooperative switched to dosing broilers with our bulk tablets after low-yielding flocks indicated missed subclinical parasitism. Within three growth cycles, flock uniformity and feed conversion improved measurably. Similarly, a racing stable managing mature horses documented fewer reinfestation events and less reported colic after switching from generic batches to our directly supplied tablets and premix solutions.
Dairy farmers working under export restrictions have told us that our batch-level documentation and responsiveness to custom sizing requests made a direct impact on their ability to maintain compliance for EU-bound exports. Tablet manufacturers focusing on companion animal health have noted reduced “out of specification” events in chewable and flavored formulations when switching to our consistent supply, lowering waste and quality deviation costs.
Not all animal APIs behave the same. Water solubility, reactivity with tablet excipients, and batch-to-batch taste have each impacted the market entry of pyrantel-based generics and their long-term adoption. Our in-house veterinary advisor assists in bridging the gap between chemical quality and in-vivo clinical outcomes, visiting partner factories to review issues in person and recommend practical improvements. It’s a hands-on approach rooted in manufacturing, not just sales.
Global supply interruptions and increases in counterfeit or diluted APIs in the veterinary sector threaten animal health and undermine customer confidence. By keeping all synthesis and finishing on-site, we have countered this risk. Recent years have seen more inquiries from buyers seeking assurance of full traceability, given high-profile product recalls in other animal drug classes. Some buyers bring their own raw material evaluators, and we open factory doors to guided tour audits, chemistry reviews, and blind sample draws from real production lines.
As regulatory scrutiny rises around undeclared by-products or allergens in animal feed and medication, we have responded with extra layers of internal QC and routine independent lab testing. It is not just about compliance—it is about accountability, protecting veterinarians and end users from unexpected outcomes or reputational damage. Knowing the buck stops with us sharpens focus at every step.
Purchasing decisions for animal health actives cannot rest on price or certification alone. The active ingredient chain is only as strong as its manufacturing base. As a team, we have seen the patterns of global price-driven shortages, where poorly managed supply chains resulted in fake or adulterated APIs reaching the market. We have improved our own crisis preparedness, investing in reserve stock, redundancy in key process equipment, and frequent upskilling for staff. Field failures cost everyone in the chain–from farm to retail, and ultimately in lost consumer trust.
Manufacturers selling animal health actives direct to finished dose producers shape the standard for safety and performance in regional and global markets. We have built-up direct working relationships with veterinary colleges and clinical researchers. They bring back real-world feedback on resistance patterns, clinical response, and occasional formulation challenges. Our job is to close the loop, translating field data into upstream improvements, not to rest on generic specifications or broad claims.
Animal health is more than a formula. It is shaped by honest communication, rigorous process controls, and a refusal to cut corners. Formulators, veterinarians, and farmers—all trust that the active API in a tablet, solution, or feed additive will meet its claim, mix exactly as intended, and perform predictably. Our Pyrantel Pamoate stands out because it consistently meets those expectations, forged over years in the pressure-cooker of daily production and practical field application.
Drawing on the practical experience gained from thousands of batches, our continuous improvement mindset means tomorrow’s Pyrantel Pamoate will be even better than today’s. We have introduced more robust inline monitoring tools, advanced impurity profiling techniques, and initiated research projects with local technical colleges aimed at reducing environmental footprint and energy usage across the process. Our investment in new particle engineering and drying equipment supports not only higher yields but sharper control over every batch parameter that matters to final product performance.
We keep lines of communication open with every sector of the veterinary drug market: animal clinics, private label feed brand owners, academic researchers, and regulatory compliance teams. Real-world feedback—whether a minor flow issue in tablet presses or a solubility challenge in a new oral gel—feeds back into manufacturing, leading both process and mindset upgrades. The next generation of animal drugs demands even more stringent quality attributes, and we are investing now to match and exceed these expectations.
Our manufacturing team takes pride in every API batch that leaves the facility. We see ourselves as partners with every veterinarian, farmer, and pet owner relying on those tablets or solutions. From raw chemical synthesis through careful quality control and on to finished dose recommendations, our focus stays on safety, consistency, and straightforward delivery of what matters: protection from parasites, improved animal well-being, and peace of mind.
Pyrantel Pamoate Tablets in veterinary grade result from a system of care, expertise, and responsibility built up over years, not just a process on paper. Our partners in the animal health supply chain trust us because they have seen the difference between solid and weak supply. Having full control over our manufacturing, from initial synthesis to the moment the API ships, matters not just for us, but for every link in the animal health value chain. We remain committed to supporting clients—formulators, veterinarians, large herd owners, pet clinics—by delivering reliable, transparent, and responsive supply of Pyrantel Pamoate, proven in the factory and the field.