Products

Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    • Product Name: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions
    • Alias: albendazole-tablets-veterinary-grade-api
    • Einecs: 252-057-8
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    653172

    Product Name Albendazole Tablets Veterinary Grade API
    Chemical Formula C12H15N3O2S
    Appearance White to off-white crystalline powder
    Intended Use Veterinary
    Dosage Forms Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions
    Mechanism Of Action Inhibits microtubule synthesis in parasites
    Solubility Practically insoluble in water
    Purity Typically ≥ 98%
    Shelf Life 2 to 3 years when stored properly
    Storage Conditions Store in a cool, dry place away from light
    Cas Number 54965-21-8
    Molecular Weight 265.33 g/mol

    As an accredited Albendazole 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 & Storage
    Packing Albendazole Tablets Veterinary Grade, 1,000 tablets, sealed HDPE bottle, tamper-evident cap, labeled with dosage, batch, and expiry details.
    Shipping Albendazole Tablets (Veterinary Grade API) are securely packed in moisture-proof, tamper-evident containers or fiber drums lined with double-layer polyethylene bags. Shipments are dispatched via air or sea with protective insulation, accompanied by requisite documentation and MSDS. Transit complies with international standards to ensure product integrity and quality upon delivery.
    Storage Store Albendazole Tablets (Veterinary Grade API) in a tightly closed container, protected from light, moisture, and excessive heat (below 30°C). Keep in a dry, well-ventilated area away from incompatible substances. Ensure the storage area is secure and properly labeled. Avoid exposure to direct sunlight and keep out of reach of children, animals, and unauthorized personnel.
    Application of Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    Purity 99%: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with purity 99% is used in broad-spectrum anthelmintic treatments for livestock, where it ensures optimal parasite eradication efficiency.

    Particle Size ≤10 Micron: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size ≤10 micron is used in oral suspension formulations, where it provides enhanced bioavailability and rapid absorption.

    Stability Temperature up to 40°C: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with stability temperature up to 40°C is used in premix feed additives, where it maintains chemical integrity during storage in varied climates.

    Moisture Content <1%: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with moisture content <1% is used in powder and granule premixes, where it prevents caking and preserves shelf life.

    Melting Point 208°C: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with melting point 208°C is used in injectable formulations, where it ensures thermal stability during sterilization processes.

    pH (1% Solution) 6.5-7.5: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with pH (1% solution) 6.5-7.5 is used in oral tablet production, where it prevents gastric irritation in animals.

    Solubility in DMSO: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with solubility in DMSO is used in veterinary research solutions, where it facilitates experimental dosing and formulation development.

    Heavy Metals <0.002%: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with heavy metals <0.002% is used in capsules for high-value livestock breeds, where it ensures product safety and regulatory compliance.

    Residue on Ignition <0.2%: Albendazole Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with residue on ignition <0.2% is used in injectable preparations, where it minimizes unwanted insoluble residues for safe administration.

    Free Quote

    Competitive Albendazole 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.

    For samples, pricing, or more information, please contact us at +8615365186327 or mail to admin@ascent-chem.com.

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    Tel: +8615365186327

    Email: admin@ascent-chem.com

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    Certification & Compliance
    More Introduction

    Albendazole Tablets Veterinary Grade API for Animal Health: A Manufacturer’s Insight

    Meeting the Demands of Modern Animal Health

    Years of manufacturing active pharmaceutical ingredients for veterinary use have shown that challenges in animal healthcare never stay still. Albendazole stands out among the antiparasitic agents our industry relies on, acting as a key tool in protecting livestock health and productivity across the globe. Our expertise starts from the raw synthesis of albendazole—handled in GMP-compliant, tightly controlled environments—to the careful particle sizing and blending for precise, effective dosing in tablets, powders, premixes, and solutions.

    Veterinarians and producers face shifting parasite resistance, stricter regulations on residues, and rising pressure to keep cycles efficient. From our vantage in the plant, we see demand for not just ‘albendazole,’ but a trustworthy, versatile API tailored for compressed tablets, oral solutions, and premixes. That’s where our value comes in: our product is not generic albendazole powder off the mill; it goes through multiple stages of micronization, impurity monitoring, and stability confirmation, designed for the unique technical requirements of each finished dose form.

    Specifications and Consistency Every Step of the Way

    Consistent product starts with tight control over every processing stage. The veterinary albendazole API is produced for broad-spectrum, oral and injectable uses, including:

    Our production focuses on pharmaceutical-grade purity, tight residual solvent levels, and low heavy metal content. Because this API serves as the starting material for critical veterinary products, each batch is subjected to more scrutiny and quality checks than broad-market technical albendazole. The particle size distribution is adjusted to match the finished product—finer for bolus and oral solutions, coarse as needed for granules. Appearance, odor, and bulk density are all monitored so granulators, tablet presses, and capsule fillers in our clients’ facilities can run smoothly. Factories often forget that poor powder flow or variable crystallinity costs downstream, so we keep physical characteristics within narrow targets.

    Why Veterinary Grade Albendazole Demands Its Own Approach

    Many products on the market come from generic chemical plants, aimed for quick commerce rather than animal health. Livestock producers and veterinarians have long demanded APIs that hold up under field conditions, without erratic dosing or unpredictable dissolution. Albendazole produced for feed premixes must tolerate blending, moisture variations, and remain bioavailable after weeks in finished feed. Tablets for use in sheep must disintegrate almost instantly. Poorly controlled supply leaves too many variables—broken dosing, retreatment failures, and even detection of unwanted residues that threaten a processor’s entire lot.

    In veterinary medicine, performance on farm matters as much as paperwork. Factory-fresh API, stored under nitrogen and tracked for temperature shifts, simply handles better in real-world processing. Our lots are layered with process documentation, tracking every day and every batch through to tableting, solution blending, or granulation. This gives our partners data they can use in regulatory filings, not just a material certificate or generic analysis.

    Experience Matters: Responding to Market and Regulatory Shifts

    Albendazole’s applications range from large dairy herds to single animal treatments in companion animals. Over the years, international guidelines on veterinary APIs have tightened, with new requirements for residual limits, excipient compatibility, and even anti-counterfeit traceability. We didn’t just watch regulations change—we invested in new assay equipment, additional stability chambers, and full-spectrum impurity profiling in response.

    We monitor our output for albendazole sulfoxide and sulfone impurities, residual solvents, dioxins, and even trace isomer formation unique to high-pressure synthetic processes. This approach moved beyond what’s adequate for crop protection or basic treatment. These parameters don’t just please regulators; they also guard against sudden field failures or downtime in partner facilities.

    We ship product that fits not only domestic policies, but anticipates U.S., EU, Australian, and major Asian requirements. Some partners require tailored batch sizes, or additional stability data under tropical and subtropical conditions. Years of feedback tells us what causes tablet breaking during shipping, or delays in solution clarity, and we solve these at the manufacturing stage, not after.

    Real Differences From Commodity Albendazole

    Not every albendazole API behaves alike. Commodity technical-grade products, sold by traders for general chemical use, carry more variability in their physical and chemical profile. Lower purity, higher moisture sensitivity, and batch-to-batch shifts often show up during final processing or, worse, out on the farm through visible failures. Our veterinary API sticks to its own lane, designed with actual finished formulation use in mind.

    For clients switching from generic grades, the gains become obvious fast: Fewer runs of dust, smoother tablet pressing with unchanged punches, and less residue in granulators. Finished veterinary medicine stays on label for its dissolution and stability profile, and, when doctors request test data, our batches match what is on file—not just one-off reference lots. This cuts the cost and time spent retesting and reprocessing.

    Our team fields call-backs not just from purchasing agents, but from animal health R&D heads, who want to know how our manufacturing process lets them shorten their own laboratory scale-up. We routinely support stability studies for partners exporting to hot climate regions, providing real-word data on shelf life that generic supply chains can’t match. This runs not as an extra service, but as an essential part of keeping the animal health sector running in today’s fast-shifting global market.

    Supporting Innovation in Veterinary Formulations

    The market now needs veterinary APIs that let manufacturers develop new, bioavailable, and user-friendly veterinary products. Albendazole must be ready for chewable forms for companion animals, as well as slow-release injectables or water-dispersible powders for large-scale farm use. Our plant technology adapts with every new trend: spray-dried dispersions and tailored particle fractionation are options for customers pursuing specific delivery technologies. We train our team in new compaction, granulation, and film-coating needs—because our API must keep pace with the goals of formulating partners and regulators.

    We also maintain a technical service team with years of hands-on tableting, mixing, and animal trial experience. If a batch presents handling trouble or an unexpected shift in color or odor, we trace the source within our process logs. Several long-term partners have sent their formulation teams through our plant to see firsthand why consistent upstream control translates to lower formulation costs and faster batch releases. For producers facing audits or product recalls linked to variable API, this detailed process transparency becomes a major reason for loyalty.

    Delivering for Animal Health, Not Just Compliance

    Field veterinarians and farm managers don’t have time or tolerance for repeat dosing or confusion over product performance. Our albendazole API starts with global reference monograph compliance, but the people using it care about actual results. Blast resistance, fast wetting, and consistent bioavailability are all features we refine lot after lot. That starts with strict plant hygiene, closed-system processing, and prompt dispatch.

    Our clients have told us the difference they see in feed mill application, where powder must keep a steady flow rate for automated bagging, or in large-scale tableting where downtime from binder incompatibility costs more than the API itself. Consistency across lots turns into direct savings on service calls, batch re-release testing, and finished product warranty claims. Over time, we found strong field performance leads to better relationships—veterinary clients ordering directly, trusting that what ships matches specification and performs predictably.

    What Industry Experience Has Taught Us

    Manufacturing albendazole at scale reveals issues that specs alone don’t capture. Fines content, temperature sensitivity, and even oxygen exposure during storage can affect both formulation and finished product performance. Over decades, we revised our plant layout, invested in new air drying and inert gas storage, and recalibrated our dynamic blending process after each round of customer feedback. Unlike generic chemical supply, this attention allows us to adjust supply to fast-changing demand, keep reserve stocks stable, and pivot if a regulatory body releases new compliance targets.

    Experience tells us that manufacturing for the animal health sector isn’t just business as usual; it requires deep coordination between our technical, quality, and logistics teams. Shortfalls in one plant, delays in container shipping, or raw material supply constraints get resolved quickly—regular buyers stay informed and rest assured that critical feedlots and clinics don’t run dry. No matter the scale of order, each batch receives the same hands-on care and mandatory final inspection.

    Frequent site audits by regulatory authorities keep us up to date and honest. Plant managers and laboratory technicians participate directly—witness signoffs, real-time deviation reporting, and root-cause investigations when parameters deviate. Our record stands up to long-term review, not just cursory batch results.

    Upholding Safety and Sustainability

    Due to resistance and environmental concerns, many markets now demand clear information on residue profiles, breakdown kinetics, and safe disposal for all veterinary agents. Our manufacturing method minimizes generation of hazardous byproducts, and uses continuous closed-cycle water recovery systems. Waste stream reduction and on-site incineration cut overall impact, in line with the goals of responsible animal health production. Our chemists analyze both finished API and plant effluent regularly, adapting process chemistry to keep pollutant levels within safe, approved limits.

    Veterinary APIs inevitably end up in the environment through animal waste, pasture treatment, and even from accidental spills. By taking direct responsibility at the point of manufacture, we can play our part in reducing risks to non-target wildlife, downwind water sources, and human food safety. Working with university partners and public laboratories, we continuously refine our degradation models and develop new monitoring techniques for active metabolites in the field. This practical responsibility extends not only to the animals dosed, but to consumers, landowners, and surrounding habitats.

    Building Trust With the Veterinary Medicine Community

    The animal health industry faces scrutiny unlike any other. Every year, regulators push for tighter residue limits, new identification standards, and improved traceability—all with input from agricultural experts, veterinarians, and food safety authorities. We take these developments as shared challenges, not just regulatory hurdles. By keeping production documents traceable, making batch test results available for regulatory dossier filing, and responding quickly to audits, our manufacturing plant supports veterinarians and producers with transparent, defensible supply.

    Our onsite analysts frequently engage animal health clients to explain not just what’s in the delivered API, but how its measured content relates to withdrawal times, livestock application schedules, and companion animal safety. This direct line opens long before any product ships, so practical, solution-oriented feedback comes in at every stage. Pharmaceutical-grade outputs get followed up with after-sale check-ins, root-cause support for formulation issues, or new application guidance from the laboratory. This loop of support goes beyond what’s found in standard bulk chemical sales; it stands as a foundation of long-term partnership.

    Adapting to End-User Expectations

    Over recent years, the demands from downstream veterinary medicine manufacturers have evolved. More look for APIs ready for advanced delivery platforms, like chewable doses, unique feed premixes, or slow-release bolus forms. Others focus on bulk powder blends that reach hundreds or thousands of animals at once, making large-scale consistency more critical than ever.

    Sometimes, the challenge rests on solving for new sensitivity to allergens or excipient incompatibility, as market priorities change. More end-users require clear, accessible chain of custody records, demonstrating every stage of production. Our personnel track release samples to the smallest factor—ambient humidity logs, storage temperature, and process deviation reports—all bundled for client reassurance.

    Albendazole Veterinary Grade: Making the Difference in Animal Welfare

    A sound API, produced and monitored from start to finish within a single plant, means more than a specification sheet. It means stronger odds of successful parasite management, fewer headaches over regulatory recalls, and better outcomes for both food suppliers and veterinarians. Our manufacturing approach keeps the focus on how the product works in the hands of the people that rely on it every day, not just on paper.

    As those responsible for the whole lifecycle of our albendazole—from its chemical synthesis to its finished form—we believe direct manufacturing control brings practical gains for everyone using or relying on veterinary medicine. Facing shifting disease threats, tighter legal controls, and higher end-user expectations, experience and responsiveness make the difference. Our commitment always keeps animal health at the center, sustaining results for the producers, handlers, and veterinarians across the industry.

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