Products

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

    • Product Name: Andrographis Herba Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions
    • Alias: andrographis-herba-veterinary-grade-api
    • 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

    851374

    Product Name Andrographis Herba Veterinary Grade API
    Appearance Fine greenish-brown powder
    Botanical Source Andrographis paniculata
    Purity ≥98% by HPLC
    Active Ingredient Andrographolide
    Intended Use Veterinary medicinal preparations
    Solubility Partially soluble in water, soluble in ethanol
    Dosage Forms Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions
    Storage Conditions Store in a cool, dry, and dark place
    Shelf Life 24 months if unopened
    Country Of Origin China
    Packaging 25 kg fiber drum or as required
    Cas Number 5508-58-7
    Moisture Content <5%
    Standard Complies with veterinary pharmacopeia

    As an accredited Andrographis Herba 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 Sealed 25kg fiber drum with double-layer PE bags inside, clearly labeled "Andrographis Herba Veterinary Grade API" for pharmaceutical manufacturing.
    Shipping The chemical **Andrographis Herba Veterinary Grade API** is securely packaged in fiber drums or double-layer polyethylene bags, ensuring product integrity during shipping. It is shipped in cool, dry, and well-sealed containers, with all necessary labeling and documentation provided for safe handling in tablets, injections, capsules, powders, granules, premix, and solutions.
    Storage Andrographis Herba Veterinary Grade API should be stored in a cool, dry, and well-ventilated area, protected from direct sunlight and moisture. Keep the container tightly closed and away from incompatible substances. Store at room temperature, ideally below 25°C. Ensure the storage area is secure and restricted to authorized personnel only, following all local regulations for veterinary pharmaceutical ingredients.
    Application of Andrographis Herba Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions

    Applications of Andrographis Herba Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions in Industrial Manufacturing

    As an advanced manufacturer, we supply Andrographis Herba Veterinary Grade API meeting strict veterinary and pharmaceutical production needs. Our material supports a variety of downstream manufacturing routes for animal health formulations, with strict compliance and process integration for global export and local large-batch production.

    1. Veterinary Oral Powder Formulations for Livestock

    Feed manufacturers apply this API in the formulation of water-soluble oral powders for ruminants, swine, and poultry. These powders serve anti-infective and anti-inflammatory purposes, particularly in large-scale farming environments. Producers ensure mixing uniformity with carriers such as dextrose or starch, then perform drying, sieving, and packaging operations meeting veterinary GMP tools.

    Industry compliance standards

    • China Veterinary Pharmacopoeia (2020 Edition) requirements for oral formulations
    • EU Regulation (EC) No 1831/2003 for feed additives and veterinary APIs
    • Veterinary Good Manufacturing Practice (vGMP) regulations applicable locally
    • Feed Hygiene Regulation (EC) No 183/2005

    Typical usage ratio

    • Ranges from 0.2% to 2.0% API depending on target animal and disease profile
    • Adjustment based on herd size, oral uptake rates, and solubility requirements

    Downstream process integration

    • Added during premixing with carriers
    • Homogenized in ribbon or paddle blenders
    • Passes through granulation or direct powder compaction before final dosing
    • Filled and sealed in multi-layer foil bags or PE containers

    Final product types

    • Water-soluble oral powder sachets for livestock
    • Bulk powder blends for on-farm dosing
    • Premixes for further integration into compound feeds
    • Dosage packs for veterinary clinics

    2. Veterinary Injectable Preparations

    Formulation companies use Andrographis Herba API in sterile injectable solutions for animal health, especially where parenteral treatment is required for systemic infections in cattle, swine, and companion animals. Processes include dissolution in sterile vehicles, adjustment to isotonicity, filtration, aseptic filling, and sterilization by autoclaving or filtration.

    Industry compliance standards

    • US FDA Guidance for Industry #230 – Compounding Animal Drugs from Bulk Drug Substances
    • European Pharmacopoeia Monograph 1381 for injectable preparations
    • GMP for veterinary sterile products (e.g., 21 CFR Part 211 or EU GMP Annex 1)
    • WHO guidelines on non-human pharmaceutical manufacturing

    Typical usage ratio

    • Usually between 0.1% and 1.0% API by solution volume
    • Dosing varies by target species and product labeling

    Downstream process integration

    • API dissolved in buffered saline or glucose solution
    • Filtered under sterile conditions (0.22 μm)
    • Ampoules or vials filled in aseptic suites
    • Terminal sterilization or final filter-sterilization practiced as per batch protocol

    Final product types

    • Sterile single-dose or multi-dose vials
    • Pre-filled syringes for veterinary use
    • Large-volume (100–500 ml) bottle formulations for herd treatment
    • Hospital-packaged injectable solutions

    3. Veterinary Tablet and Bolus Manufacturing

    API is compressed into solid dosage forms such as tablets or boluses for ruminants and equines. Production involves granulation with excipients (lactose, MCC, or starch), blending with lubricants, tablet compression, and often a protective film coating for stability in field conditions.

    Industry compliance standards

    • China Veterinary Pharmacopoeia and local animal drug monographs
    • ISO 9001:2015 and FAMI-QS for animal pharmaceutical manufacturing
    • Veterinary Drug Administration Law (China) for dosage manufacturing
    • Industry-specific shelf-life and stability protocols

    Typical usage ratio

    • Formulations typically contain 1%–10% API per tablet (variable by animal bodyweight needs)
    • Formulator alters API load to manage release rates and single-dose requirements

    Downstream process integration

    • Dry or wet granulation stage entry
    • Compression to target hardness in rotary tablet presses
    • Optional sugar, film, or enteric coating applied post-compression
    • Bulk and retail blisters or high-volume bottles sealed for shipment

    Final product types

    • 10 g boluses for cattle and horses
    • Chewable flavored tablets for companion animals
    • Small-dose (0.5 g) tablets for poultry and swine
    • Blister-packed dosage units for field veterinarians

    4. Veterinary Capsule Production

    Downstream producers employ our API in the manufacture of hard-shell and softgel capsules for animals requiring precise dosing or oral administration with enhanced palatability. Granules or powders containing the API blend with flow aids and stabilizers before encapsulation and quality control for uniformity.

    Industry compliance standards

    • Veterinary medicinal product guidelines under Council Directive 2001/82/EC (EU)
    • US FDA Guidance for Industry on medicated capsules for non-food producing animals
    • Veterinary Production License (China)
    • ISO 22716 for Good Manufacturing Practices

    Typical usage ratio

    • API content per capsule ranges from 0.2% to 8% according to capsule size and animal species
    • Dosage tailored based on bodyweight and intended treatment period

    Downstream process integration

    • API blends in V-blenders or fluid bed granulators before capsule filling
    • Encapsulation on semi-automatic or high-speed rotary machines
    • Weight variation and content uniformity testing on each batch
    • Bottling with desiccant and labeling for traceability

    Final product types

    • Gelatin capsules for canine and feline therapies
    • Large-volume powder capsules for ruminants
    • Softgel capsules containing API in lipid carriers
    • Multi-compartment capsules for complex dosing regimens

    5. Medicated Feed and Premix Manufacturing

    Premix feed mills incorporate the API during the blending of high-volume medicated premixes for commercial feed operations. This application targets intestinal and respiratory health in poultry, pigs, and aquatic animals. The process includes API weighing, dry blending with mineral/vitamin bases, and micronization to guarantee uniform distribution across tonnage batches.

    Industry compliance standards

    • Regulation (EU) 2019/4 on the manufacture of medicated feed
    • Code of Federal Regulations (21 CFR 558) for medicated animal feed (US)
    • Hazard Analysis and Critical Control Points (HACCP) certification
    • Feed Additive Directive 70/524/EEC

    Typical usage ratio

    • Commonly 0.01% to 0.5% API in final feed premix
    • Levels depend on withdrawal periods and animal target species

    Downstream process integration

    • API introduced during premix blending after base minerals and vitamins
    • Screening to eliminate agglomerates
    • Micro-dosing units control API distribution in high-throughput lines
    • Packing in multi-wall sacks or flow bins for transport to compounders

    Final product types

    • Medicated feed additive premix for poultry
    • Starter and grower medicated meal for pigs
    • Fish and shrimp pellet premix with specified API content
    • Bulk medicated vitamin/mineral blends

    6. Veterinary Granular Solution Preparations

    Formulation plants prepare granular concentrate products with the API for on-farm dilution or direct administration through water lines. Granulation processes involve agglomeration with binders, drying, and particle size control to optimize solubility and dispersibility in water systems under practical farm conditions.

    Industry compliance standards

    • Pharmacopoeia of the People's Republic of China – Veterinary part
    • ISO 22000 food safety management for animal feed/medicine intersections
    • EFSA (European Food Safety Authority) guidelines for animal medicated water administration
    • Veterinary GMP batch record management

    Typical usage ratio

    • API content adjusts between 1% and 12% in concentrate depending on dilution protocol
    • Mix ratio set per animal daily water intake and required dosing duration

    Downstream process integration

    • API mixed with binder and carrier in high-speed granulators
    • Drying and sieving to reach required mesh size for fast dispersal
    • Granules packed in water-proof multi-layer sachets
    • Clear labeling for on-farm safety and administration control

    Final product types

    • Aqua-administered granular solutions for pig and poultry farms
    • Granular concentrates for large livestock dosing tanks
    • Measured sachets for two-step water dilution
    • Multi-dose farm pack formats

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    Email: admin@ascent-chem.com

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    Certification & Compliance
    More Introduction

    Andrographis Herba Veterinary Grade API: A Manufacturer’s Perspective on Quality and Application

    Our Approach to Making Andrographis Herba API for Animal Formulations

    For years, we have been turning Andrographis paniculata into an active pharmaceutical ingredient (API) that serves a clear purpose in veterinary medicine. Through our own extraction and purification lines, Andrographis Herba has become a raw material that fits real-world applications: tablets, injections, capsules, powders, granules, premix, and oral solutions for animal health. Since we produce from the ground up, each order reflects the actual needs we hear from veterinarians and animal feed formulators, not just a catalog spec.

    When the raw herb arrives, our teams handle every stage—thorough cleaning, controlled drying, and extraction under conditions that keep the andrographolide content within the target range. Over years in manufacturing, we have learned where each batch can drift based on crop source and harvest window, so we test for actives at every step. Our technical staff constantly adjusts extraction cycles and filtration points to keep the final powder within consistent specification, always keeping an eye on trace contaminants and solubility.

    How Manufacturing Method Affects the API

    Different final products call for slight differences in the physical properties of the Andrographis Herba API. We control particle size distribution to match the needs for tablets, capsules, or pellets, as fine powder improves blending for premixes, while granules may increase stability in some feed additive forms. Our spray-dried powder goes through micronization, so it disperses more cleanly with excipients for even compounding in tablets and capsules. The amorphous or crystalline forms can alter how quickly the actives release in water or oil-based suspensions—something that matters in injectable or oral solutions.

    We take pride in running tests for residual solvents, pesticide residues, and heavy metals after every lot. Our scale of production allows us to dedicate certain lines to veterinary API only, reducing risks from cross-contaminants. Staff get regular training to avoid mix-ups between veterinary and human API processes, which is crucial as regulations for animal health become more rigorous worldwide.

    What Sets Veterinary API Apart from Human-Use Grade

    Veterinary API gets made to handle tougher real-world scenarios than human-use grades. Premixes can face extended transport under warm warehouse conditions and may be stored at the farm in open bins. For this reason, we focus on stability under heat and humidity. Water solubility tests are performed in the kinds of water available on farms, not just ultra-pure lab water: this gives us feedback on realistic dissolution rates.

    Feed manufacturers need product that disperses quickly, without causing sediment issues or blockages in automated dosage systems. Some forms of our API pass fluidization tests, simulating large-scale premix handling. In comparison, our human API requires more stringent limits on microbial purity and solvent residues, but veterinary batches must tolerate harsher end-use conditions. There is sometimes a trade-off in excipient selection; for injection grades, we avoid certain animal-derived carriers, and provide documentation for BSE/TSE-control.

    Where We See This API Used Most Effectively

    Andrographis Herba powder is being integrated into multi-component veterinary medicines for livestock and companion animals with a focus on promoting healthy gut function, reducing fever, supporting immune response, and maintaining resilience during transport or after vaccination. Pork, poultry, and aquaculture operations seek anti-inflammatory support that comes from botanical origin. From our dialogue with veterinarians, the most common response is that Andrographis-based injectables and oral solutions fill a gap during outbreaks of bacterial and viral challenges, especially with limits on antibiotic use.

    Recent field reports describe improved recovery rates when Andrographis API is part of a controlled trial alongside standard supportive care. This feedback leads us to tune specifications for faster solubility or improved dispersibility based on the intended route of administration and animal type.

    What Makes Andrographis Herba a Unique Choice in the Veterinary Market

    Farms and feed mills face ongoing pressure to reduce their reliance on traditional antibiotics and chemical coccidiostats. Plant-based actives, like those in Andrographis Herba, have attracted growing interest because of their broad spectrum benefits and lower risk of drug resistance or residues in animal products. Our experience producing to veterinary specification means customers get a material that’s ready to deploy—either blended into custom formulations or packed as a single-ingredient premix.

    Feedback from swine and poultry producers points to measurable drops in unthriftiness and post-weaning diarrhea when Andrographis supplements are on hand for stressful periods. Since our production facilities operate under quality assurance programs recognized for veterinary API, we track stability under sunlight, as products may be stored outside or in non-air-conditioned feed sheds. Working with animal nutritionists, we adjust carrier compounds to keep products free-flowing, preventing sticking in production lines.

    Differences Between Our Andrographis API and Generic Sources

    We often meet veterinarians who have experienced poor results with inconsistent Andrographis from general herb traders or feed brokers. These issues commonly arise from wide variability in active marker content and problems with microbial quality. In our operation, all batches go through precise HPLC quantification for andrographolide, and we keep batch records that link marker content to crop supply chain. Direct partnerships with select growers allow us to map potency back to field location and seasonal variation.

    Our APIs are also made to tight particle size range, documented for each shipment, and supported by certificate of analysis from our own labs. For products destined for registration or tender in regulated markets, we provide more analytical data—residual solvent, loss on drying, ash content, even extended heavy metals screening. Our veterinary customers know that a batch from us behaves as expected in their final product, unlike bulk herb powders that arrive with poorly defined properties.

    To support antibiotic-free claims in animal farming, we offer non-GMO and organic-compliant lots. Our facility operates an allergen-control program, and our records trace each lot to select Andrographis sources. This documentation helps feed manufacturers respond to audit demands or export requirements.

    Solving Real-World Formulation Problems

    Animal health companies often reach out with specific problems: powders that won’t blend, granules that cake, or uneven dosing in mass-medication protocols. Our technical team frequently gets involved at the formulation stage to help customers solve these bottlenecks. For example, by adjusting moisture content or using cold granulation, we create a flowable product even in high-humidity climates. Tablets that require rapid disintegration get a blend with a tailored excipient matrix.

    In oral solutions and injectable suspensions, we have refined the pH buffers and carrier agents so that active content dissolves fully at the point of use, without visible residue or clumping that could clog equipment. Our water solubility checks take into account common farm water impurities, not just distilled water, giving a more practical picture of field performance.

    Years of direct conversations with end-users—sometimes at a crowded farm office or a noisy feed plant—have shaped the practicality of our Andrographis API lines. Problems like odor masking or browning of formulations have been reduced after tweaking upstream drying stages or including antioxidants at the right dosage.

    Advantages of Working with a Direct Manufacturer

    Purchasing Andrographis Herba API straight from the line, not via trade intermediaries, means supply chains are shorter and quality feedback comes faster. Any batch close to expiry can be traced, recalled, or replaced directly. We keep samples of all outgoing lots on site, making it possible to troubleshoot issues quickly if anything unusual appears at the customer end. Engineers and QC staff are at hand to tweak a run in response to a new need—no need to wait cycles for technical approvals from external traders.

    Customers often ask us to match a new market standard, like an absence of certain colorants or a new analytical detection method. Our in-house R&D group runs parallel analysis and tweaks process flow until the product fits the target. This real-time process adaptation delivers value and traceability to those making label claims about origin, active percent, or compliance with a regional veterinary Dossier.

    Understanding the Regulatory Perspective

    Across continents, veterinary product registration standards grow more rigorous every year. To meet modern demands, our facilities have designed documentation and tracking to reflect both Chinese and international regulatory frameworks for veterinary APIs. Every production lot is accompanied by a batch record and full traceability starting from field harvest through final drying, testing, and packing. We respond directly to customer audits and regulatory site visits, keeping physical and electronic records available for real-time inspection.

    Many customers require support with dossier development or technical analytics for new-country registrations. Our technical team can provide validated analytical methods, stability data under accelerated and real storage conditions, and information on origin and supply chain integrity. Batches for the European or North American market require even more exhaustive pesticide screening, limits on genotoxic impurities, and support for toxicology profiles. In these cases, we support clients with documentation packs that cover not just standard product analysis but also environmental risk and batch-to-batch impurity profiles.

    Veterinary products must, in many cases, survive complex logistics routes, sometimes with products spending weeks outside climate control. Our manufacturing controls attempt to forecast these stresses, so that Andrographis Herba API survives real-world challenges, not just ideal storage. Customers for oral, injectable, or feed premix APIs receive guidance on proper mixing and storage drawn from our decades of follow-up experience.

    Improving Formulations: Practical Input from Our Laboratory

    Over time, we see frequent trends in customer feedback—some tablets require better hardness, injections need more stable suspensions, or powders must survive long journeys through hot, humid weather. Our R&D team works on pilot-scale batches in the same way end-users manufacture, using tableting, mixing, and granulation technologies similar to those in feed mills and veterinary drug plants.

    Every time we solve a new issue—whether it’s a caking powder shipment or a batch that dissolved too slowly in a field test—we refine our in-house procedures. Improvements like smaller particle size, enhanced moisture control, or a refined solvent removal phase balance batch-to-batch consistency with process efficiency. We believe that living close to the manufacturing process, and open feedback from every link in the user chain, builds a product that is reliable on farms and in finished medicines.

    Environmental and Crop Source Aspects

    The future of botanical APIs in veterinary uses depends not only on extraction technology but also on responsible cultivation. We work closely with partner farms in areas that yield high andrographolide-bearing plants. Regular visits to growers help us fine-tune guidance on pesticide application, harvest timing, and post-harvest handling, sharpening active content and ensuring a responsible environmental footprint.

    Our technical team screens each herb delivery for pesticide residues and heavy metals before taking it through the manufacturing process. Because veterinary APIs can end up in the food chain, we observe not just product purity checks but also regulatory standards for withdrawal periods and residue monitoring, working with customers to support their documentation needs.

    Customer-Focused Support: Real-Time Solutions for Real Problems

    Customers count on fast response for product questions, technical clarifications, or supply chain challenges. Our team provides live updates on each production run, from test results and packing status to shipping conditions and estimated time of arrival. When batches face delays at customs or get stuck on the road, we offer documented support to minimize downtime at the feed mill or animal health facility.

    If a new regulation or internal compliance requirement appears, customers get updated data and certificates, not empty reassurances. Feedback loops with manufacturing and laboratory staff ensure that each lot meets expectations for ease of use, dispersibility, and stability. Field issues are relayed directly to technical and production teams, leading to process improvements that filter back into new lots.

    From a practical standpoint, continuous engagement with animal health professionals, feed manufacturers, and veterinary product developers means we refine our production with every market demand. It is not enough to meet a one-time spec; long-term users need consistency, traceability, and honest communication about what can and cannot be achieved with a botanical API.

    Perspectives on the Future: Opportunities and Challenges in Veterinary Botanical APIs

    Our experience shows growth in demand for botanical API, especially as new markets restrict the use of old-guard pharmaceuticals in animal husbandry. Countries around the world seek robust alternatives that support animal performance without contributing to resistance issues or creating regulatory hurdles on export. Regulatory frameworks for veterinary botanical products are evolving, and strict documentation for every shipment—source, process, and analytic—has become the standard.

    We anticipate more pressure to refine extraction processes, improve active recovery, and operate within tighter environmental controls. Training and investment in technical staff remains a priority, as process and regulatory requirements shift year by year. Transparency, direct feedback, and close partnership with both upstream growers and downstream users shape the success of Andrographis Herba API in the global veterinary sector.

    New product developments in veterinary medicine—whether fast-disintegrating tablets for companion animals or stabilized powders for aquatic farm systems—continue to set higher expectations for what a botanical API must deliver. The ability to adapt, scale, and innovate remains central to our manufacturing approach. We value each opportunity to learn from the field, adjust our process, and contribute to safer, more sustainable animal health products worldwide.

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