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HS Code |
907509 |
| Product Name | Pseudostellariae Radix Veterinary Grade API |
| Source | Pseudostellaria heterophylla root |
| Application | Veterinary use |
| Formulations | Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions |
| Main Ingredient | Pseudostellariae Radix extract |
| Appearance | Off-white to brownish powder |
| Solubility | Water soluble |
| Purity | ≥98% (HPLC) |
| Shelf Life | 2 years if properly stored |
| Storage Conditions | Cool, dry place, protected from light |
| Usage | Raw material for animal pharmaceuticals |
| Packaging | 1kg/bag, 25kg/drum or customized |
| Country Of Origin | China |
As an accredited Pseudostellariae Radix 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 | Pseudostellariae Radix Veterinary Grade API is packaged in 25 kg double-layered fiber drums, inner polyethylene bag for moisture protection. |
| Shipping | Shipping for **Pseudostellariae Radix Veterinary Grade API** is conducted in secure, tamper-evident packaging to preserve quality and prevent contamination. The product is dispatched via reliable logistics partners, with temperature and moisture controls as required. All shipments include comprehensive documentation and comply with international regulations for safe pharmaceutical transport. |
| Storage | Store Pseudostellariae Radix Veterinary Grade API in a cool, dry, and ventilated area, away from direct sunlight, moisture, and heat. Keep the container tightly closed and protected from contamination. Avoid exposure to incompatible substances. Store at room temperature and ensure proper labeling. Keep out of reach of unauthorized personnel, and follow all relevant local regulations for storage of veterinary APIs. |
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Purity 98%: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with purity 98% is used in oral dosage formulation, where it ensures high bioavailability and consistent pharmacological activity. Particle size D90 < 50 μm: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size D90 < 50 μm is used in powder and granule preparations, where it promotes uniform dispersion and rapid dissolution. Moisture content < 2%: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with moisture content < 2% is used in capsule and tablet production, where it improves shelf-life and storage stability. Melting point 165°C: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with a melting point of 165°C is used in premix and solution manufacturing, where it supports thermal stability during processing. Microbial limit < 100 CFU/g: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with a microbial limit < 100 CFU/g is used in injection preparation, where it ensures safety and reduces contamination risk. Stability temperature 25°C: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with stability temperature at 25°C is used in long-term storage scenarios, where it guarantees maintenance of therapeutic properties. Heavy metals < 10 ppm: Pseudostellariae Radix Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with heavy metals content < 10 ppm is used in veterinary product formulation, where it complies with regulatory safety standards. |
Competitive Pseudostellariae Radix 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 as a manufacturer of botanical veterinary API has shaped our standards, and Pseudostellariae Radix stands as a testament to the value of commitment and detail-driven processes. Year after year, feed and veterinary pharmaceutical producers ask for consistency in particle size, moisture, and bioactive content to meet strict process parameters and ensure batch-to-batch reproducibility. Our Pseudostellariae Radix veterinary grade API addresses these ongoing needs across tablets, injections, capsules, powders, granules, premix, and solutions.
Decades in the sector reveal that even small differences in granule size or extract ratios make their way into downstream processing and animal response. Many buyers have tried “generic” alternatives and reported issues like dusting during tableting, poor dispersibility in premixes, and unpredictable dosing for injections or solutions. Our technical teams have worked side by side with formulators to establish requirements based not only on published compendia but on practical bench testing and long-term field data. That’s why we calibrate our extract ratios, water solubility, and sieve sizes tightly for the veterinary line—fine enough for sterile injectables, stable for liquid premixes, and compressible for direct tableting. Raw herb selection, multi-stage extraction, filtration, and drying controls—all are monitored to give a reliable input for downstream pharma, not just “herbal powder.”
Our veterinary production line produces several models, covering both full-spectrum powdered root and standardized extracts. The main differences lie in the degree of concentration and drying, with options like concentrated powders at 5:1 or 10:1 extract ratios. Granule size options range from fine 80 mesh for injectables and capsules to coarser 40 mesh for oral premixes. This detailed grading isn’t an afterthought. We’ve found laboratories consistently flag API from unregulated sources for failing to meet microbial or foreign matter thresholds. Our process strictly controls microbial loads and keeps residual solvents below market detection limits. Water content is kept under 5% to prevent caking or degradation during storage, particularly critical for long-cycle logistics or bulk warehouse storage in fluctuating climates.
Pseudostellariae Radix is used in animal health to support immune function, appetite, and recovery—applications that require precision. Tablet producers report lower rejection rates when using our material due to improved flow and direct compressibility, and veterinary injectable producers achieve repeatable solubility for their solutions without surprise sedimentation. In poultry, swine, and companion animal blends, consistent batch behavior means less time adjusting premix formulations. Our customers have sent feedback—once skeptical veterinarians now spot gradual improvement in convalescent or stressed animals, especially during feed transitions or seasonal illness waves. This feedback loop from farms and clinics to our quality teams drives continuous adjustments and improvements in our process.
Producers and feed mills face relentless pressure on cost and traceability. We invest heavily in raw material verification, chromatographic QC, and lot-level traceability, so our veterinary API never leaves questions about adulteration or batch inconsistency. It’s common knowledge in the manufacturing world that Pseudostellariae Radix from some “bulk” suppliers arrives with unknown fillers or synthetics—practices that risk product recalls and damage to veterinary brands. Inspection cycles throughout our process catch and remove off-spec material. Each production run is logged with origin data, so producers meet both local and export requirement audits. Over the years, we’ve seen brands knocked back at customs for unclear botanical traceability. Our records—root harvest zones, batch chromatographs, and independent third-party validations—help bypass these hurdles.
Veterinary requirements differ sharply from human dietary supplement needs. Most consumer-grade Pseudostellariae powder is ground for oral blends or traditional medicine decoctions, where particle size or trace excipient levels don’t matter as much. In contrast, veterinary use often requires strict solubility and compound release profiles. API for injectables cannot contain insoluble fiber or unexpected tannin content, and granulation for animal capsules or feed formulations fails with excess fine dust or clumping. We control every critical variable, from moisture and ash content to extract solvent residues, so formulators get a predictable API that integrates smoothly into both advanced and traditional dosage forms.
Veterinary APIs need to withstand inspection from both internal site audits and external regulatory authorities. Some countries require GAP traceability, others specify maximum allowed pesticide residues or mycotoxin levels. Since the regulatory environment changes, our process includes routine screening for known contaminants and heavy metals. Quality goes beyond just an internal spec sheet. As manufacturers, we’ve learned customers rely on timely, transparent data. So, each outgoing lot includes detailed documentation and verifiable data—not just a COA, but test results from accredited laboratories. Lapses in documentation have disrupted shipments for others in the field; for us, it’s a lesson learned.
Direct customer feedback shapes our approach more than any external guideline. When a vaccine producer reported filter clogging with an early lot, we re-examined filtration processes and adjusted our grinding line. Feed additive customers ask for free-flowing material so their bulk blending lines stay efficient, so we calibrate moisture and granule size closely. For capsule manufacturers, color stability and low oxidative degradation help maintain shelf appeal and avoid off-color batches. Each time a recurring issue emerges, our lab team tracks the root cause and makes changes to upstream or on-line controls. This process of iterative improvement—listening, adjusting, and validating—creates API that matches real-world veterinary demands.
New veterinary markets put pressure on producers to offer safe, sustainable, and traceable alternatives to synthetic feed additives. Pseudostellariae Radix, with carefully controlled extraction and screening, supports these broader goals. It offers a plant-based API free from antibiotics, free from genetically modified markers, and meets tightening rules on animal product traceability. Years of shipping both domestic and export orders give us a sense of market dynamics and what formulators watch for—stability, data, and customer-facing transparency. This is more than a commodity. Each kilogram links back to a controlled production process.
Our position at the raw material source gives us influence over harvesting and ecological practices. Unchecked wildcrafting of Pseudostellariae has caused shortages and environmental damage in some regions. We contract with established growers and participate in local sustainability initiatives, ensuring long-term availability. By working directly at the farm level, we reduce unwanted herbicide exposure and keep pesticide residue below the allowed veterinary thresholds. Careful sourcing also matters for product consistency, with single-origin batches displaying much narrower content variations compared to blends from multiple locales. This upstream control helps veterinary brands avoid sudden profile changes in finished product.
Bulk handling brings its own challenges. Large-scale dosage manufacturing and premix blending require robust packaging to prevent moisture ingress or contamination. We supply the API in food-grade, multi-wall bags or drums with tamper-evident seals. Veterinary customers report fewer transit losses and reduced caking, even with intercontinental transit. Packaging units are sized for direct use in production lines, so opening a drum or bag provides consistent material for immediate batch processing, not a mix of fines and clumps that need secondary handling.
Support often determines whether a supplier becomes a long-term partner or just another vendor. Our technical service team roots solutions in hands-on production experience. Customers facing tablet capping or inconsistent fill weights receive production-oriented feedback—from adjusting excipient rates to slight modification in blending or granulation. A direct line of communication links our QC and lab staff with partner R&D teams, creating a real-time technical loop. Solutions come grounded in what works at scale, not just theoretical guidelines.
Pseudostellariae Radix veterinary API faces scrutiny from site inspectors, import authorities, and brand-level quality review boards. Our manufacturing documentation supports compliance in North American, European, and Asian veterinary regulatory systems without friction. There is no room for ambiguous batch certificates or unverified botanical claims. Each shipment incorporates bilingual documentation, with digital traceability linking every kilogram to its field and process origin. This foundation supports veterinary brands as markets open new distribution channels or introduce products in jurisdictions with evolving botanical ingredient requirements.
The veterinary sector faces constant change—feed regulations evolve, animal health standards adapt, and consumer pressure for transparency drives higher levels of scrutiny. Our approach consists of ongoing monitoring and incremental upgrades rather than static specs. Customer input, independent audit results, and colloquial feedback from feed mill operators and veterinary clinics all contribute to refining processes and expanding documentation depth. Rather than shipping “one-size-fits-all” bulk powder, this results in a diverse and targeted lineup of API grades for a wide range of dosage forms.
Healthy livestock underpin global food security and sustainable animal agriculture. High-quality inputs to veterinary pharmaceuticals and nutritional supplements mean veterinarians and feed formulators can offer effective, safe, and proven support for animal health. Our Pseudostellariae Radix veterinary grade API directly supports these aims—delivering reliable plant actives in a format built for modern manufacturing, all backed by supply chain transparency and batch-level verification. Across thousands of batches shipped each year, our focus lands on supporting both animal outcomes and manufacturing efficiency.
Decades of manufacturing for the veterinary sector have made it clear: one-off orders rarely create value. Our partnerships run deep—coordinated planning for future harvests, advanced notice on regulatory changes, and joint troubleshooting of process headaches for new dosage forms. As a direct manufacturer, we build in time to discuss “out-of-spec” problems, unexpected formulation incompatibilities, and potential cost optimizations. This means veterinary brands get more than a bulk API supplier—every order is a node in a wider relationship that ties quality control, regulatory compliance, and business logic together.
Pseudostellariae Radix veterinary grade API, in our experience, works best not just as a product but as part of a collaborative ecosystem—linking manufactures, formulation teams, veterinarians, regulatory agencies, and end-users. Our ongoing focus on empirical quality, documentation, and sustainability ensures that finished dosage manufacturers receive both practical support and a dependable, authentic product.