API

SORBITOL 70% TS02 is a clear, colourless, syrup liquid and it is miscible with water. It can be used as a moisturizer or sweetener in food, personal care, and health care. It is also an important raw material for industry.

Urapidil Base is a white crystalline powder. When dissolved, it forms a clear, colorless solution that is free of particles.

Products still subject to third-party patent protection might be available solely for R&D purposes.

Nadifloxacin: Advanced Antibacterial Solution Refarmed Chemicals presents Nadifloxacin, an efficacious fluoroquinolone antibiotic designed for the assured treatment of various bacterial infections. With its potent broad-spectrum activity, Nadifloxacin offers healthcare professionals a robust option for combating Gram-negative and Gram-positive bacteria, that are often responsible for conditions such as urinary tract infections (UTIs), skin and soft tissue infections, respiratory tract infections, and certain sexually transmitted infections (STIs). Nadifloxacin's pharmacological profile indicates it is generally administered orally via tablets or suspension, with dosing regimens from 500-1000 mg every 12 hours, though this may adjust based on infection severity and individual patient requirements. This medication underscores its commitment to quality and safety, presenting a product that is white to yellowish in crystalline powder form, ensuring high purity with an assay value of ≥ 99.0%. Made with stringent adherence to Good Manufacturing Practice (GMP) standards, Nadifloxacin is both soluble and stable in various solvents, including sodium hydroxide TS and N,N-dimethylformamide (DMF), offering versatile formulation options. Its melting point ranges from 246-250°C, emphasizing its stability under a broad spectrum of conditions. Clarity and color of the solution are maintained as clear, colorless to slight yellow, with stringent checks on impurities – including heavy metals and arsenics kept to minimum levels, aligning with industry standards. While side effects can include nausea, vomiting, diarrhea, and other conditions, they are closely monitored, ensuring optimal patient safety. Patients with hypersensitivity, seizure histories, or on interfering medications are advised to avoid this product and consult healthcare professionals. Nadifloxacin's efficacy is matched only by Refarmed Chemicals' attention to detail and commitment to patient health. With transparent documentation and certification, consumers are assured of the product's integrity, supplemented by the comprehensive information provided by the DKSH Group to facilitate informed decision-making. As a corporate customer looking to source reliable antibiotics, Nadifloxacin represents a high-grade pharmaceutical ingredient that stands for efficacy and safety in the management of bacterial infections.

Products still subject to third-party patent protection might be available solely for R&D purposes.

Ketotifen Hydrogen Fumarate is a specialized pharmaceutical compound with profound implications in the management of allergic conditions. As a white to off-white crystalline powder, it embodies the archetypal pharmaceutical intermediate that serves a critical role in the synthesis of medications aimed at mitigating allergic symptoms. This compound, with the molecular formula C19H19NOS·C4H4O4 and a molecular weight of 425.50 g/mol, is an epitome of pharmacological innovation, designed to alleviate discomfort associated with allergic rhinitis and conjunctivitis, while also playing a preventive role in asthma management. Fabricated with meticulous precision, Ketotifen Hydrogen Fumarate is both soluble in water and ethanol, ensuring versatility in its application for medical formulations. With a melting point between 160-163°C, where it starts decomposing, this substance remains stable under a wide range of conditions, ensuring a dependable shelf-life for pharmaceutical products. When handling this product, adherence to stringent safety guidelines, including the use of personal protective equipment, is imperative to minimize potential contact risks. It demands storage in cool, dry environments, shielded from light and moisture, to preserve its integrity. Respected for its non-sedating nature, Ketotifen distinctively works by inhibiting the discharge of histamine and other mediators from mast cells, thus curtailing the cascade of allergic reactions without inducing significant drowsiness. The side effects are minimal, with mild drowsiness, dry mouth, and nausea being among the most common, while more severe reactions such as confusion or hallucinations are decidedly rare. An advocate for quality and safety, Refarmed Chemicals, a leading pharmaceutical ingredient manufacturer, assures regulatory compliance, with Ketotifen Hydrogen Fumarate approved by the FDA for prescribed use. As such, corporate customers seeking a reliable cornerstone for their allergy-treating formulations will find this product to be a formidable addition to their pharmaceutical repertoire.

Products still subject to third-party patent protection might be available solely for R&D purposes.

Pizotifen Maleate, presented by Refarmed Chemicals, is an instrumental pharmaceutical agent aiding in the management of several health conditions. Its primary use is in the prevention of migraines, a debilitating headache disorder known to impair the quality of life. Furthermore, it serves as a reliever for vestibular disorders, which include symptoms such as vertigo, dizziness, and tinnitus. In addition to these, Pizotifen Maleate has proven effective in treating pruritus, chronic itching skin conditions, and acts as an adjunctive therapy for asthma, providing relief from respiratory discomfort. Manufactured under stringent quality control conditions in India, Pizotifen is carefully crafted into tablets with dosages of 5 mg and 10 mg to accommodate varying therapeutic needs. The active ingredient is a histamine antagonist, functioning by obstructing histamine receptors in the body, hence mitigating inflammation and associated symptoms like itching. It is essential to note that while Pizotifen Maleate is generally well tolerated, common side effects might include drowsiness, dizziness, dry mouth, nausea, and occasional headaches. Due to its drowsing effects, this medication should be used cautiously, particularly when concentration is required, such as in driving or operating heavy machinery. Exercise caution before using Pizotifen Maleate if any of the following conditions are present: glaucoma, prostate enlargement, narrow-angle glaucoma, or any known hypersensitivity to the drug. Additionally, individuals with liver or kidney complications should consult their healthcare provider before commencing treatment. Stored ideally at room temperature, Pizotifen Maleate should be shielded from light and moisture. Full efficacy may take several weeks to establish, making it imperative to adhere to the prescribed dosage regime. In the occurrence of severe adverse effects, the treatment should be discontinued, and medical advice must be sought immediately. Each batch of Pizotifen Maleate undergoes rigorous testing ensuring a high purity—exemplified by the specifications pertaining to solubility, identification tests, and the stringent control over impurities. Your corporate clients can trust in the quality sustained by EU GMP certification, as reflected in the clear documentation and reliable manufacturing processes. Choosing Pizotifen is investing in a pharmaceutical product that is as dedicated to patient wellness as it is to consistent product integrity.

Products still subject to third-party patent protection might be available solely for R&D purposes.