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HS Code |
247730 |
| Product Name | Sulfaguanidine Tablets Veterinary Grade API |
| Chemical Formula | C7H10N4O2S |
| Molecular Weight | 214.25 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Slightly soluble in water |
| Intended Use | Antibacterial agent for veterinary applications |
| Administration Forms | Tablets, Injections, Capsules, Powders, Granules, Premix, Solutions |
| Shelf Life | 2-3 years when properly stored |
| Storage Conditions | Store in a cool, dry place away from direct sunlight |
| Cas Number | 57-67-0 |
As an accredited Sulfaguanidine 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 | White, high-density polyethylene bottle with a tamper-evident cap, labeled 500 Sulfaguanidine Tablets (Veterinary Grade, 500mg each), batch and expiry details. |
| Shipping | Sulfaguanidine Tablets, Veterinary Grade API, are securely packed in moisture-resistant containers or drums. Each batch is clearly labeled and shipped via regulated, temperature-controlled transport to ensure product stability. Packaging conforms to international standards and includes necessary documentation for safe handling, storage, and regulatory compliance during transit. |
| Storage | Store Sulfaguanidine Tablets (Veterinary Grade API) in a tightly closed container, protected from moisture and light. Keep in a cool, dry place at temperatures below 25°C. Ensure the storage area is well-ventilated and away from incompatible substances. Keep out of reach of children and animals. Follow all local regulations and safety guidelines for pharmaceutical storage. |
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Purity 99%: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with purity 99% is used in the formulation of veterinary oral tablets, where it ensures superior antimicrobial efficacy against gastrointestinal infections. Particle Size <50 microns: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with particle size less than 50 microns is used in premix animal feed supplements, where it promotes uniform dispersion and improved bioavailability. Moisture Content <1%: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with moisture content below 1% is used in injectable veterinary solutions, where it enhances product stability and reduces risk of hydrolysis. Melting Point 195–198°C: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with melting point 195–198°C is used in production of soluble veterinary powders, where it provides consistent dissolution properties. Stability Temperature up to 40°C: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions stable up to 40°C is applied in the preparation of veterinary capsules, where it ensures shelf-life and activity retention during storage. Solubility in Water >10 mg/mL: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with water solubility over 10 mg/mL is used in oral solution preparations for livestock, where it facilitates rapid drug administration and absorption. Bulk Density 0.45–0.55 g/cm³: Sulfaguanidine Tablets Veterinary Grade API for Tablets / Injections / Capsules / Powders / Granules / Premix / Solutions with bulk density of 0.45–0.55 g/cm³ is used in granule veterinary formulations, where it enhances homogeneity and dose consistency. |
Competitive Sulfaguanidine 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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Manufacturing pharmaceuticals for animals takes a blend of experience and honest materials. Our work with Sulfaguanidine API began years ago and it still holds a central place in animal health. After seeing countless production lines, testing runs, and farm results, I can say Sulfaguanidine has earned its reputation among veterinarians who face frequent cases of intestinal infections, especially bacterial dysentery and enteritis, across livestock and poultry. It is not magic—just reliable chemistry, time-tested by daily farming practices.
Demand always dictates innovation, but what keeps us grounded are the clear signals from the field. Customers, mostly long-serving farm veterinarians and pharmaceutical companies, show a preference for veterinary-grade Sulfaguanidine when seeking cost-effective, robust first-line support. Treating farm animals, especially in herd situations, leaves little room for products that do not perform every time. Farm health can swing rapidly if an infection breaks out and delays in production or inconsistencies in powder or tablet performance cannot be tolerated.
Our Sulfaguanidine for veterinary use comes as an Active Pharmaceutical Ingredient (API), carefully tailored to match common dosage forms: tablets, injections, capsules, powders, granules, premixes, and liquid solutions. This flexibility is not just a matter of recipe changes. Getting the model right means working directly with mixing engineers and pharmaceutical formulating partners. They want clean, white to off-white crystalline powders with steady particle size, satisfying the pharmacopeial standards for veterinary actives.
The core model we deliver shows high purity, strict moisture content, and minimal impurities. We monitor for polymorphic changes and degrade formation batch to batch. Many years in this business have taught us the danger of rushing process parameters or neglecting humidity controls during milling and blending. Instead of chasing a long list of possible grades or custom lots, we have refined the standard veterinary grade to provide reliable downstream performance in all the usual presentation forms.
Post-processing, the API readily compresses into strong, low-friability tablets, disperses evenly in oral powders, and remains shelf-stable during further processing into premix or injectable solution. The importance of batch consistency comes through every step—any deviation turns up first in subpar tabletting, and then as customer dissatisfaction. Everything in our process revolves around avoiding this, using real-world checks and tight traceability from raw sulfanilamide intermediates all the way to the outgoing batch of Sulfaguanidine API.
Sulfaguanidine’s primary use has always targeted gastrointestinal infections in animals: pigs, chickens, turkeys, cattle, and sheep. Most veterinarians reach for it to tackle bacterial enteritis and neonatal diarrhea—conditions that rapidly dehydrate young or stressed herds. The unique pharmacological feature of Sulfaguanidine is its limited systemic absorption in the gut. It acts locally where infections take hold, sparing the rest of the animal’s system, reducing unwanted residues in meat, milk, or eggs.
In our own post-market observations collected over years of feedback and cooperation with drug development teams, clear patterns emerge. Sulfaguanidine API, whether found in an oral bolus, drenched in a powder, or layered into a feed premix, works reliably when rapid, site-specific action is needed. It minimizes the risk of systemic adverse reactions and offers veterinarians clear withdrawal timelines. This local mechanism also allows formulation into multi-component blends for broader spectrum anti-infectives without major changes to withdrawal periods.
Many of our long-term clients, from regional corporate farms to independent feed mills, have seen that Sulfaguanidine fills a gap not easily closed by newer, systemically absorbed antimicrobials. The performance of the API in these contexts speaks for itself. In growing broiler operations or pig rearing environments, the API supports rapid return to healthy feed conversion rates and growth after outbreaks of coccidiosis or bacterial scour.
In recent years, as regulators and buyers become more focused on antimicrobial stewardship, our Sulfaguanidine model continues to offer one of the safest, least resistance-inducing choices in the toolkit, precisely because its target site limits sub-therapeutic systemic exposures.
Years of producing API for animal health products show the subtle yet meaningful differences between high-excipient, mass-market finished tablets from traders and direct-manufacturer Sulfaguanidine API. Quality always starts from the first grams out of the reactor, not in a warehouse awaiting repackaging. We control the chain end-to-end. That means no shortcut in crystallization, no tolerance for off-spec color, odor, or solubility after granulation.
Unlike some products coming from speculative brokers or import-based suppliers, our batches avoid blending leftovers or repurposed pharma waste streams. Instead, our teams run dedicated lines for veterinary Sulfaguanidine, allowing tight management of cross-contamination—from early-phase batchwork to drying, sieving, and final API packaging. Many customers have asked for API certificates and batch samples, not just paperwork. These conversations remind us of the difference between real, accountable manufacturing and generic bulk reselling.
Many partners also encounter products on the market carrying inconsistent particle sizing or excipient pre-mixes. These variants cause poor blending in animal feeds or uneven suspension in injectables. Only by running regular in-house tests—particle size distribution, flow properties, water content, and real-world press trials—do we confidently state differences. Reliable Sulfaguanidine surfaces as a pure, stable, easily handled powder, rather than a tentatively blended composite labeled as API by brokers far removed from any production.
Antibiotic resistance pressure also gives Sulfaguanidine API an edge. Where more complex sulfonamides or combination therapies introduce cross-resistance concerns for veterinarians and regulators, our API’s gut-limited action reduces selective pressure on broader animal microbiota. Our own animal trial data suggest steady downward trends in resistance when customers maintain correct dosing and observe withdrawal periods. Each kilogram we ship gets documented by unique batch control numbers, supporting real traceability from milled raw sulfanilamide to the finished package.
Efficient pharmaceutical teams want easy, predictable integration of API into their tablets, soluble powders, capsules, and feed additives. After spending years side by side with development scientists—even mixing test blends during on-site visits—we know that the Sulfaguanidine model must hit tight moisture content, compressibility, and flow properties or the entire production lag behind. With animal health, batch failures do not just mean lost money but can leave a whole production setup without viable inventory at the wrong moment.
All chemists fight the same fight against cross-batch contamination, caking, and degradation, especially in hot or humid regions. Sulfaguanidine’s stability is well-documented, but even a low level of allowed impurities can stress coating processes or affect downstream palatability. Our approach fixes these points, keeping the number of excipient, stabilizer, or color-addition variables to a minimum. This translates to less batch-to-batch reworking and fewer surprises at customer QA laboratories.
A typical veterinary API request, for example, might require a 10% blend granule for use in poultry feed—here, our Sulfaguanidine’s consistent density and wettability produce no surprises during test extrusions or subsequent mixing. If a partner requests API suitable for injection, the low endotoxin, low particulate profile means smooth filtration and aseptic processing, again verified in small-scale pilot runs at our facility side-by-side with client teams.
Real manufacturing always comes down to the reliability of checks—both in the plant and outside it. Our technical team routinely samples each lot for pH, residual solvents, and heavy metals, checking against the standards set by veterinary pharmacopeias. Investments in up-to-date HPLC and GC infrastructure ensure no human error slips past in this phase. QA and QC processes do not stand on ceremony; they rely on operators who are familiar with the profile of good Sulfaguanidine from years of hands-on practice.
The traceability chain starts from the sulfanilamide base, moving through each transformation, with real-time logging of reactor conditions and filtration cycles. The warehouse never holds untracked stock, nor do we accept material for blending from outside uncontrolled sources. The downstream products reflect that commitment—stable, low-dust powders, high-yield tablets, and uniform granules. Delivering on-time, intact batches is more than logistics; it is the result of every step, from ingredient weighing to controlled environment storage.
We stand ready to answer technical questions with batch samples, analytical data, and in some cases, in-person visits to local plant floors. Over the years, veterinary clients have called us directly—not brokers—to troubleshoot mixing challenges or give advance notice of changing formulation needs. That direct channel builds a feedback loop, improving both the product and the production protocols over time. We record these challenges and feed outcomes back into the plant SOPs for continual updating.
From a manufacturer’s perspective, every challenge revolves around scale, batch preservation, and practical storage. In places with extreme temperature swings or long-distance distribution, the stability of Sulfaguanidine API must be proven through accelerated and real-time trials. Our packaging team has tested multiple bag liners, anti-caking agents, and desiccants. Field results always beat theory, and we adjust based on whether bags show clumping after weeks in a shipping container or powders bounce freely on arrival at the distributor warehouse.
Dealing with global regulatory differences, we log country-specific pharmacopoeial requirements and regularly audit both in-house methods and documentation. Having our own analytical labs removes reliance on off-site testing, letting us respond faster and reassure import partners when regulatory changes occur. Only through real, eyes-on-the-API verification can we ensure the client’s blending or tableting line won’t stop abruptly due to a missed impurity or moisture drift.
Veterinary pharmaceutical needs never stand still. Disease outbreaks, supply chain disruptions, and new stewardship policies all shift the daily calculation of what works and what does not. Unlike the short-term reseller model, our approach invests in long supplier and client relationships, prefers open books, and responds to recalls or special customer requests fast. Over decades in the field, this philosophy has led to incremental improvements—better tablet hardness, quicker dissolution, stronger odor masking for offensive-tasting actives, and sturdier transport options for high-humidity seasons.
Trust is hard-earned in veterinary pharmaceuticals. A usable API results not just from specifications but from daily plant habits—how materials are stored, who runs checks, how complaints are resolved. One shipment of out-of-spec API can tarnish years of reliability and disrupt thousands of meters of production line. As direct manufacturers, we set expectations—from technical standards to packaging—to prevent this. Our best clients know someone at our end by name, able to discuss technical tweaks, storage tips, or last-minute batch reserves.
A proper manufacturer’s reputation grows by delivering usable, batch-consistent Sulfaguanidine, with real traceability and field feedback. Partners tend to remember which supplier answers on a holiday and which batch outperformed during a local health crisis. Those are the moments revealing which practices matter most—solid process controls, honest QA teams, and a healthy respect for both chemistry and field realities.
Field-driven improvement never pauses. In animal health, reacting to outbreaks means moving fast, and reliable Sulfaguanidine tablets or powders enable veterinarians to keep herds protected. Scaling production means more than meeting demand; it means holding to the same high purity, compressibility, and dissolution properties that define a solid API.
Our plant teams set up their protocol cycles around the habits learned from client demands—packaging tailored for the shipping route, mixing designed for quick dissolution, in-plant documentation that matches as-supplied and as-used conditions. By insisting on a hands-on, traceable production process, we constantly audit both quality and process safety so that our Sulfaguanidine works not just in the lab, but on the farm, under everyday stress.
No single API can answer every possible animal health challenge, but real feedback from longtime customers keeps Sulfaguanidine API improving every season. Farm veterinarians and animal pharmaceutical producers teach us which tweaks—particle size reductions, improved moisture barriers, adjusted pH—actually translate to better herd health. These lessons fuel ongoing innovation in our manufacturing, making veterinary Sulfaguanidine a steady choice amidst shifting standards, new regulations, and unpredictable field needs.
Our commitment endures: deliver quality Sulfaguanidine API, keep channels open for questions, and ground every upgrade in daily manufacturing realities. Years of partnership, not just transactions, form the backbone of dependable animal health solutions.