Veterinary medicine constantly searches for tools to manage pain, inflammation, and fever in animals. Flunixin meglumine emerged from this drive back in the late twentieth century. Researchers working to develop non-steroidal anti-inflammatory drugs (NSAIDs) for animals faced tough challenges. Options like phenylbutazone offered pain relief, but with notable safety risks, especially in equines and livestock. Flunixin began as a new approach: its parent compound, flunixin, came from the family of nicotinic acid hydrazides. By reacting this with meglumine, a sugar amine, chemists produced flunixin meglumine, a water-soluble salt. The aim: match the therapeutic promise of existing NSAIDs but with fewer adverse effects and better tissue distribution, allowing use in a broader range of livestock. By the late 1970s, flunixin meglumine gained approvals under names like Banamine and Finadyne across several markets. Its rise marked a turning point for large animal care, as veterinarians could finally address pain and swelling from surgeries, injuries, and infectious illnesses with a powerful, fast-acting tool.
Flunixin meglumine usually arrives as a fine, white to off-white crystalline powder. Its chemical formula (C14H11F3N2O2·C7H17NO5) reflects a union of flunixin, a trifluoromethylaniline derivative, and meglumine, a sorbitol-derived compound. This salt formation increases flunixin’s water solubility, making injectable and oral solutions possible. Flunixin itself offers poor solubility, so the meglumine addition isn’t just a convenience—it’s fundamental to making flunixin deliverable and effective for real-world veterinary use. Its melt point lands around 191-195°C, and it dissolves easily in water yet not in organic solvents like ether, ethanol, or chloroform. This selective solubility shapes its pharmaceutical design: solutions for injection, pastes for oral dosing, and granules for feed admixture remain the main forms for veterinary practice. Each physical product must balance chemical purity, stability for storage, and consistent dosing—critical points for regulatory approval and practical animal care.
Each label and technical sheet for flunixin meglumine spells out more than just the basic chemical details. Products usually guarantee not less than 98% purity, measuring both the flunixin base and the meglumine salt in strict proportion. Labels must clearly state the intended species, administration route (intravenous, intramuscular, or oral), and withdrawal intervals for food-producing animals. Governments set firm limits for acceptable daily intake (ADI) and maximum residue levels (MRLs) in meat or milk, considering consumer safety and export requirements. In many countries, strict batch testing tracks impurities like hydrazines or other residual solvents, with detection limits set in the parts-per-million range. Drug manufacturers also need to include specific technical instructions—recommended dosage (often 1.1 mg/kg in cattle and horses), frequency, and contraindications. Warnings for potential side effects, such as kidney risks or gastrointestinal irritation in sensitive species, feature on every package to guide veterinarians in safe and responsible use.
Synthesizing flunixin meglumine starts with flunixin acid itself, which arises by condensing a trifluoromethylaniline ring with nicotinic hydrazide, followed by forming the appropriate salt with meglumine through aqueous reaction. Industrial-scale processes demand tight controls to ensure full reaction and purification, avoiding unreacted hydrazide or organic residues. After dissolving both pieces in sterile water, they’re combined under precise pH conditions. The resulting salt crystallizes, washed and dried to minimize endotoxins or pyrogens. Modern manufacturers have pushed toward greener synthesis methods, scaling down solvent waste and recycling reagents wherever feasible. Beyond the chemical steps, GMP guidelines require tight environmental control, validated cleaning, tracked batch production, and full traceability of raw materials—global standards now reflect the growing complexity of drug supply chains and the real risks of contamination.
Flunixin’s core structure features a 2-methyl-3-(trifluoromethyl)aniline moiety linked to a nicotinic acid hydrazide, which blocks cyclooxygenase (COX) enzymes to suppress prostaglandin formation. Researchers have tinkered with esterification, amidation, and salt-forming reactions, yet the meglumine version consistently comes out on top for water solubility and biological activity in veterinary use. Flunixin undergoes extensive hepatic metabolism, generating acyl glucuronides and hydroxy derivatives which help clear the drug from the animal’s system. Any effort to develop novel derivatives must balance activity with residue concerns—modifications could slow breakdown and residue clearance, raising withdrawal times for food animals and complicating regulatory approval. Innovation leans toward prodrug development, such as encapsulating flunixin in biodegradable polymers for slower release, but current market realities push most research toward improved formulations for easier handling and better compliance in the field.
The pharmaceutical world often rebrands a molecule to match cultural, marketing, or regulatory priorities, so flunixin meglumine bears several aliases. Among veterinarians, names like Banamine, Finadyne, Flunixin Injection, and Megludyne crop up most frequently. The core molecule—sometimes sold as flunixin or by code numbers—never changes, but excipients, concentrations, and packaging shift from brand to generic or across borders. This opens competition but also brings in risks of variable quality between manufacturers. Regulatory agencies attempt to standardize potency and composition, though country-by-country differences persist. Still, Banamine and Finadyne, as pioneers of the class, built reputations backed by three decades of clinical practice, so many prefer sticking to time-tested products where budgets allow.
The reality of working with potent NSAIDs like flunixin demands respect. All storage must avoid light, moisture, and temperature extremes to preserve stability. Handlers need to wear gloves, since accidental contact or needle-stick events can cause adverse skin reactions and, rarely, systemic effects. Veterinarians know that overdosing spells trouble, from gastric ulcers and kidney strain in horses to tissue necrosis or shock with improper injection technique. In feedlots or dairies, strict protocols monitor dosage, timing, and withdrawal for every treated animal. Many governments now mandate that only licensed professionals dispense and administer flunixin to forestall both misuse and illicit residue in food products. Routine environmental site controls, with spill kits and lockable storage, help stop workplace exposures and accidental releases, while ongoing training reinforces safety and legal compliance. Having seen cases where a simple paperwork miss or hurried dosing led to contamination or animal injury, it becomes clear just how demanding operational standards really are in daily practice.
Few drugs have earned such a wide berth in veterinary medicine as flunixin meglumine. For horses, flunixin features in protocols tackling colic—a painful and life-threatening condition—where it brings pain relief and, by quelling inflammation, helps slow down shock and tissue injury. In cattle, it often proves vital during mastitis, metritis, and respiratory illness, supporting comfort and appetite to speed recovery after disease strikes a herd. Some sheep and goats receive flunixin after procedures like dehorning or castration, though small ruminants remain an emerging focus due to metabolic differences. Flunixin shines in acute settings: wound repair, dentistry, surgery, or laminitis in horses, where clinicians look for potent pain relief with a manageable withdrawal period for meat or milk. Many veterinarians rely on injectable forms, especially during emergencies, while oral pastes and granules serve as follow-ons for chronic cases or less acute pain. The drug’s effect lasts upwards of 24 hours, enabling once-daily dosing—an advantage in field conditions where treatment logistics often shape care.
Since flunixin’s debut, research has aimed to clarify not just its pain-relieving effects, but also the deeper impacts on recovery times, animal welfare, and productivity. Large-scale field trials now drive data on post-surgical recovery, fever reduction in transportation stress, and performance impacts after calfhood disease. Recent studies look at new routes, like transdermal gels, aiming to avoid injection site damage and reduce animal handling stress. Extended-release capsules and adjuvant combinations show promise for farm environments, where single-use treatments cut labor costs and boost compliance. Diagnostic technologies, like rapid on-farm drug residue assays, increasingly support the responsible rollout of flunixin in food animals, speeding up decision cycles and spot-checking for illegal residues. Regulatory research continues apace on improved metabolite tracking and clarity on sublethal effects—models now explore links between NSAID use, microbial gut health shifts, and environmental residue breakdown. The pharmaceutical pipeline remains vibrant, even as established drugs like flunixin face lifecycle extension challenges and patent expirations.
Toxicity research underpins every veterinary protocol using flunixin meglumine. Horses present unique challenges, with some animals reacting to even routine dosing via gastrointestinal complications or, less commonly, renal failure—prompting calls for more personalized, case-by-case veterinary oversight. Repeated overdose in cattle, or accidental use in animals with existing liver or kidney damage, can tip the scales toward toxicity, sometimes with subtle symptoms that only emerge after days. Regulatory scrutiny drives repeated risk assessments, with special focus on meat and milk residue levels to keep food supplies safe. In the European Union, for example, food safety agencies run rolling tests, using data from routine slaughter checks and targeted monitoring. Drug companies remain under pressure to study and report even minor adverse events. Researching metabolites and tissue persistence has pushed analytical techniques forward, using LC-MS/MS for ultra-sensitive detection, helping clear or confirm even disputed residue cases. My own experience on the research and regulatory side drives home that vigilance never stops, no matter how familiar or long-trusted a drug becomes.
Looking to the future, the world of flunixin meglumine stands at a crossroads. The demand for animal welfare keeps rising, both from consumers and regulatory authorities, who now insist on pain control as a standard of care rather than an exception. Food safety worries, with shifting rules for residue limits, make life harder for generic producers yet spur innovation in faster-clearing, residue-free NSAID analogs. As antibiotic stewardship pushes for reduced use in production animals, drugs like flunixin step in as supportive therapies for non-infectious pain and inflammation—driving their relevance far beyond their original scope. Environmental sustainability presents new hurdles: active metabolite traces in manure and run-off now fall under environmental audits, so pharmaceutical firms will need to invest in breakdown studies, alternative dosing strategies, and green chemistry techniques. The technical field is shifting toward smarter formulations—think once-a-week depots or non-invasive patches—and blockchain-ready traceability for every dose administered on a commercial farm. Change will take real collaboration between researchers, regulators, veterinarians, and producers; experience shows that only integrating lab science, field realities, and ethical progress will let flunixin’s story keep evolving for new generations of animal caregivers.
Flunixin meglumine shows up in barns and vet clinics anywhere from Kentucky race tracks to small family dairies. Vets trust it for a reason—it actually works as a powerful, fast-acting pain reliever and anti-inflammatory for animals. Horses hobbled by colic or cattle battling high fevers often get relief thanks to this drug. Most folks in animal care circles think of it as “Banamine,” the original brand name, but generic versions flood the market today.
Used as an injection or paste, flunixin meglumine blocks the effects of certain chemicals in the body, mainly prostaglandins. These chemicals play a major role in swelling and pain after injury or infection. In horses, quick dosing eases gut pain from colic and calms fevers or soreness tied to respiratory illness. Dairy and beef cattle benefit too, especially in the face of painful conditions like mastitis or pneumonia.
Too many people shrug off animal pain, assuming livestock just tough it out. Experience shows otherwise. Pain slows healing and ramps up stress. Stressed or hurting cows drop in milk yield, horses stop eating, calves fail to gain weight. There’s not just an ethical issue—there’s real economic fallout for anyone raising livestock. Several studies in veterinary medicine journals point to flunixin’s ability to cut fever after surgery or infection, shorten recovery time, and improve appetite. One research project found that colicky horses treated early had a much better shot at full recovery.
Flunixin brings a lot of good, but the needle cuts both ways. On more than one occasion, I’ve seen someone reach for it without a second thought, chasing a quick fix. Frequent or overly high doses can do more harm than good. In some rare cases, horses develop ulcers or even kidney trouble from long-term use. Cows given too much or injected in the wrong spot risk tissue damage, which can lead to losses at the processor. Regulatory folks at the FDA and USDA take drug residues seriously. With flunixin, strict withdrawal times exist to keep the meat and milk supply safe—ignoring the rules by accident or in a rush risks major fines and consumer trust.
Flunixin offers farmers and vets a tool to fight pain and swelling, but it’s not magic. Basic rules apply—read labels, stick to legal doses, work with a qualified veterinarian, and never use it as a crutch for chronic problems. Better record-keeping by producers helps prevent overdosing and makes residue tracking easier during an audit. Vets work hard to teach clients about safer alternatives for some conditions, or case-by-case supportive care that doesn’t always require drugs. Research into pain scoring and alternative therapies keeps evolving, but for now, knowing your stock and catching problems early lays the foundation for compassionate animal care.
Modern animal health depends as much on good management as a bottle of flunixin in the fridge. Clean bedding, low-stress handling, proper nutrition, and quickly isolating sick animals all play into strong recovery. When pain relief is needed, flunixin meglumine remains one of the most effective tools. Used wisely, it not only helps sick or injured animals bounce back, but also builds trust among everyone who relies on safe food and healthy livestock each day.
Flunixin meglumine gets used a lot in veterinary medicine, especially with horses, cattle, and sometimes even dogs. It’s the go-to for pain, swelling, or fever, mostly because it provides strong relief fast. But not many animal owners step back and look at what happens outside of the intended pain relief. Speaking from experience with farm animals, side effects don’t always wait for a textbook scenario—they sneak up from the blind side.
The most reliable warning sign comes from the animal’s gut. Horses seem to feel this the hardest. Owners and vets report bouts of colic, diarrhea, and even severe stomach ulcers if flunixin is handed out too freely or at the wrong dose. In cattle, you see changes in eating, and in dogs, vomiting creeps in. Think about a working horse refusing hay or a dog that just keeps throwing up—it makes a normal pain day look mild in comparison. It’s fair to call ulcers and digestive upset the most common issues. Vets usually recommend not stretching out the dosing schedule and checking for early stomach warnings, like discomfort, restlessness, or blood in manure.
Veterinary drug safety keeps circling back to the kidneys and liver because these organs do the heavy lifting to clear out drugs. Repeated or heavy doses of flunixin tip the scales and can harm these organs, even in young, healthy animals. You won’t see the damage with your eyes right away. Bloodwork usually tells the story long after the problems have started brewing. Dehydrated animals are at greater risk—a horse sweating through a hot summer or cattle that don’t have access to water all day run into kidney trouble faster. It’s smart to keep clean water in front of animals and not ramp up dosing past what is recommended, even if they seem tough.
Flunixin commonly gets injected into the muscle or vein, and most animals take it without complaint. But now and then a lump, swelling, or even infection shows up. I’ve seen abscesses pop up days after a shot, needing more treatment or draining. Sterile technique goes a long way—using clean needles, rotating injection spots, and not rushing through the injection can save a lot of future problems.
Allergic reactions scare everyone—animals included—though they don’t happen every day. Look out for hives, trouble breathing, swelling, or sudden collapse shortly after administration. Vets keep emergency drugs like epinephrine on hand for a reason, and quick action saves lives. No one wants to see their animal go through this, so it pays to stick around and monitor closely right after giving the first dose, especially if the animal hasn't had this drug before.
Flunixin meglumine can turn a miserable animal around fast. At the same time, its side effects put responsibility squarely on owners, caretakers, and vets. Good dosing, careful monitoring, and regular bloodwork back up the benefits with safety. Each animal’s needs and weaknesses are different. Open conversations with veterinarians and reading up on any drug you use help you spot the problems early, so you can keep relief and risk in balance.
Flunixin meglumine stands out for its fast pain relief and anti-inflammatory effects, especially in livestock like horses and cattle. Most people in agriculture or animal care keep a vial on the shelf. Flunixin works to bring down fever, soothe joint swelling, and make animals eat and drink again in tough moments. It hits hard and fast, which owners appreciate during colic or other painful conditions.
Giving flunixin isn’t complicated, but it demands care. Most of the time, you’ll find people giving this drug by intravenous (IV) injection in horses. Large veins in the neck are the standard choice. IV injection acts quickly, sometimes bringing an animal back from the brink in half an hour. Cattle can also get flunixin IV, but some folks still use intramuscular (IM) injection in these animals. IM injection takes a little longer to show full effects and carries a small risk of muscle site reactions, but some field situations leave you with no other decent option.
Oral paste and granules exist too, mostly for horses. Oral dosing makes sense for milder cases or when daily shots might stress out the animal. I’ve seen stubborn old geldings take the paste reluctantly but get back on their feet soon after. There’s an art to keeping their heads up and not wasting the paste. Drenching or syringe work is less stressful than more needles—if the horse tolerates the taste.
Precise dosing stays top of mind. Dosing mistakes don’t just waste money—they risk kidney and gut problems. Using a weight tape or scale and proper syringes keeps things accurate. Flunixin at high doses or for too long can cause ulcers, so most vets recommend using the lowest effective dose and stopping as soon as the animal stabilizes.
Keeping product cool and sealed keeps it effective. Light and temperature swings degrade the medicine. I make a habit of checking expiration dates before every use, since old stock loses strength. Vials and syringes need to stay clean. Dirty technique brings in bacteria and more headaches than the original illness.
Veterinary prescription is more than a legal hoop—experienced oversight catches potential interactions, allergies, or underlying issues hidden beneath classic symptoms. I’ve learned the hard way not to cut corners or skip a vet call when in doubt. In food-producing animals, withdrawal time is not just red tape; it reduces the chance of drug residues in milk or meat. Regulatory agencies watch flunixin levels closely—violations mean lost sales, fines, and, more importantly, loss of public trust.
Teaching better injection skills and providing more guidance through mobile vet services could help reduce errors in remote areas. Many farmers want to learn but need practical demonstrations, not just a pamphlet. Community workshops, videos from vet universities, and on-farm training help spot problems early and prevent them from getting out of control.
Flunixin meglumine delivers relief where it counts, but sloppy handling spells real trouble. Hands-on experience, honest respect for its risks, and professional support make all the difference for animal health and safety.
Flunixin meglumine pops up often in conversations between veterinarians and livestock owners. Farmers and equestrians alike consider it a go-to option for reducing pain and inflammation. It’s stood the test of time in many veterinary cabinets. Though used so often in cattle and horses, people sometimes overlook its risks for other species. Based on my years helping out on farms and shadowing at clinics, the story isn’t as straightforward as many suspect.
Each animal species deals with drugs differently. Both the tiny lapdog and the beefy Holstein steer feel pain, but their bodies process medications uniquely. Flunixin has FDA approval for certain livestock and horses. Used right, this drug can ease colic pain in a horse, control endotoxemia, or reduce swelling from infection. In cattle, veterinarians reach for it after injuries or during respiratory disease outbreaks. Even sheep might receive it for acute pain, though with more caution. Most vets won’t use flunixin routinely on species where safety research has not been done, such as goats, cats, or ferrets.
For example, dogs can suffer severe side effects if a single dose matches the levels used in cattle. Anecdotes from the clinic remind me how easily a pain reliever for one can become harmful for another. Some dogs have developed kidney failure after treatment, which taught me early in my vet experience to read up on every drug, not trust a blanket approach. Cats have even more trouble. Their livers handle drugs much differently than other mammals, giving flunixin a high potential for toxicity even at low doses.
Livestock drugs must pass extra tests because people eat the animals. Withdrawal times come into play here. After flunixin administration, farmers must keep animals out of the food chain for a certain period. In the US, strict rules cover cattle and swine, but no withdrawal time exists for goats or sheep. An old neighbor learned this lesson the hard way, facing trouble selling sheep after a vet treated them “just like cattle”—the drug showed up in residues, and the packer turned the whole shipment away.
Evidence keeps piling up that off-label use isn’t safe without proper studies. In one published trial, flunixin persisted much longer in goat meat than beef, raising questions about food residues and consumer safety. Regulatory bodies flag these gaps, but the problem remains in many rural clinics where clients request “the same shot the cows got.”
Whenever I’m asked about pain management in animals outside the approved list, I push for honest talk with the vet. Trying something “known to work” can turn one problem into three. For non-livestock animals, veterinarians now reach more often for alternatives with proven records, like meloxicam for sheep and goats, or different NSAIDs for pets. The science pushes us to pair experience with up-to-date facts, not just habit.
The bottom line: Flunixin isn’t a one-size-fits-all answer. Care teams earn trust by sticking to research-backed guidelines and clear communication. Education keeps the right drugs in the right bodies and dangerous shortcuts off the farm. As someone who has learned from mistakes and successes alike, I believe truly caring for animals means respecting what makes each one unique—metabolism, species, and all.
Veterinarians know flunixin meglumine as a powerful anti-inflammatory and pain reliever for animals like horses and cattle. It treats everything from fevers to colic. The label on every bottle spells out the standard dose: for horses, usually 1.1 mg per kilogram of body weight, given once daily, as a slow intravenous injection; for cattle, 1.1 to 2.2 mg per kilogram, depending on the illness. This amount often relieves pain and fever effectively in routine care.
Owners sometimes ask if they can adjust the dose. A desire to ease suffering makes this understandable. But upping or stretching out the dose doesn’t always bring better results—and can cause lasting harm. For instance, flunixin is tough on the stomach and kidneys. Overdosing runs up the risk of ulcers, kidney trouble, and even death. Keeping the dose in the recommended range protects organs and gives the pain relief it’s meant to offer.
Having worked beside vets and ranchers, I’ve seen where fortunes shift with a bottle of flunixin. Say a horse colics and the barn gets tense. The urge to give more for faster relief kicks in. A wise vet checks the weight, the last dose, and any other drugs in the system. They explain that pushing past 1.1 mg/kg won’t banish pain quicker, but it will bring on new issues. Respecting the math, even under pressure, protects the animal.
Some farmers try to dose by eye, measuring out what looks right for a 1,200-pound steer. Guesswork misses the mark too often. Recent findings in animal health journals point out that nearly a third of overdoses come from estimation instead of calculation. A scale (or a proper tape measure for weight) cuts that risk. If the animal is already on another non-steroidal anti-inflammatory drug (NSAID), doubling up can do real harm. Each medicine piles on stress to the system.
Food and Drug Administration guidelines shape these doses. Authorities make those calls after looking through stacks of data on how the med moves through a horse’s or cow’s system. Veterinary studies confirm that 1.1 mg/kg, once a day, works for pain and fever and keeps side effects manageable. Anything above that limit brings more danger than reward. Below that level, many animals just won’t find relief.
Sticking to prescribed timing also matters. Giving flunixin more than once a day can keep the blood levels too high, raising the risk for side effects. There’s value in writing down every shot or dose on a barn chalkboard or notebook, avoiding double-dosing when the night gets busy.
Many problems spring from communication gaps and guesswork. Simple steps can keep animals safe. Using a digital scale instead of a rough guess makes the dose right. Posting clear dosing charts in the barn stops confusion when people change shifts. Digital record-keeping apps designed for farms cut out scribbled notes that get lost.
Education goes beyond handing out bottles. Explaining what a wrong dose means for an animal’s health—kidney failure, ulcers, or withdrawal time for food-producing animals—keeps people honest. New research points toward lower, equally-effective doses in some rare cases. That research needs to circulate quickly, but always through a veterinarian’s advice.
Flunixin helps animals get back on their feet, but it does its job best when the instructions match science and experience. Owners and vets working closely make the difference, lesson by lesson, dose by dose.
| Names | |
| Preferred IUPAC name | 2-[[2-methyl-3-(trifluoromethyl)phenyl]amino]nicotinic acid; 1-deoxy-1-(methylamino)-D-glucitol |
| Other names |
Banamine Finadyne Flunixamine Prevail Equileve Flunixin |
| Pronunciation | /fluːˈnɪksɪn məˈɡluːmiːn/ |
| Identifiers | |
| CAS Number | “42461-84-7” |
| Beilstein Reference | 1718734 |
| ChEBI | CHEBI:50177 |
| ChEMBL | CHEMBL1418 |
| ChemSpider | 163944 |
| DrugBank | DB01396 |
| ECHA InfoCard | 14e2c5d0-bde1-4651-97a2-4e12263f52e5 |
| EC Number | EC 3.1.1.61 |
| Gmelin Reference | 818977 |
| KEGG | D01066 |
| MeSH | D004017 |
| PubChem CID | 5389612 |
| RTECS number | MU7175000 |
| UNII | 2S3O079QNF |
| UN number | UN3249 |
| Properties | |
| Chemical formula | C21H28FN3O7 |
| Molar mass | 491.50 g/mol |
| Appearance | A clear, colorless to pale yellow solution. |
| Odor | Odorless |
| Density | 1.225 g/cm³ |
| Solubility in water | Freely soluble in water |
| log P | 0.3 |
| Acidity (pKa) | 1.65 |
| Basicity (pKb) | 7.83 |
| Magnetic susceptibility (χ) | -6.47e-6 cm³/mol |
| Refractive index (nD) | 1.563 |
| Viscosity | 12.45 cP |
| Dipole moment | 3.05 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 395.6 J·mol⁻¹·K⁻¹ |
| Pharmacology | |
| ATC code | QM01AG92 |
| Hazards | |
| GHS labelling | GHS07, GHS08 |
| Pictograms | GHS06, GHS08 |
| Signal word | Warning |
| Hazard statements | Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation. |
| Precautionary statements | PRECAUTIONARY STATEMENTS: Not for Human Use. Keep out of Reach of Children. |
| NFPA 704 (fire diamond) | 2-3-1 |
| Flash point | 142.6°C |
| Autoignition temperature | 187°C |
| Lethal dose or concentration | LD50 (Rat, oral): 175 mg/kg |
| LD50 (median dose) | LD50 (median dose): 175 mg/kg (IV, mouse) |
| NIOSH | NO |
| PEL (Permissible) | Not established |
| REL (Recommended) | 2 – 2.2 mg/kg PO, IV, IM, q12–24h |
| IDLH (Immediate danger) | Not listed. |
| Related compounds | |
| Related compounds |
Flunixin Meglumine Flunixin meglumine sodium Flunixin meglumine hydrochloride |