Products in Healthcare & Pharma: Binder

Kollidon® 25 SD3 serves various functions such as an anti-crystallizing agent, binder, filler, matrix-forming agent, and solubilizer. It is available in powder form and falls under the domain of pharmaceutical and nutraceuticals technologies. This product finds applications in other pharmaceutical manufacturing processes and pharmaceutical processing.

Kollidon® 30 LP, presented as a powder, serves as a binder and stabilizer. Positioned in the healthcare and pharma markets, it finds application in oral and topical drug delivery and care solutions. Suitable for various dosage forms such as capsules, granules, suspensions, and tablets, with manufacturing technologies including direct compression and wet granulation.

Kollidon® 30 SD3 functions as an anti-crystallizing agent, binder, filler, film former, matrix-forming agent, and solubilizer. It falls under the domain of pharmaceutical and nutraceutical technologies. This product finds applications in various pharmaceutical manufacturing processes and other pharmaceutical manufacturing applications.

Kollitab™ DC 87 L is a versatile pharmaceutical and nutraceutical solution. Serving as a matrix-forming agent, lubricant, disintegrant, binder, and filler, it excels in healthcare and pharma applications, specifically in drug delivery and care solutions for oral use. Available in granules, powders, and solid forms, Kollitab™ DC 87 L integrates seamlessly into pharmaceutical and nutraceutical formulations.

Kollidon® VA 64 Nub2 serves multiple functions as an anti-crystallizing agent, binder, filler, film former, matrix-forming agent, and solubilizer in the pharmaceutical and nutraceutical domains. It is available in powder form and is extensively utilized in various pharmaceutical manufacturing applications and pharmaceutical processing. This product is predominantly used in the healthcare and pharma markets, showcasing its versatility in diverse applications within the pharmaceutical industry.

Ludipress® LCE presents a granulated excipient formulation composed of lactose monohydrate and Povidone K30 (Kollidon® 30). This product comprises a white to slightly yellowish, free-flowing powder specifically crafted for direct compression applications. It boasts an odorless nature and offers a neutral taste profile. Developed with specific functionalities in mind, Ludipress® LCE finds utility in chewable tablets and lozenges, serves in effervescent tablet production, and operates as a bulking agent in hard gelatin capsules. Its roles encompass acting as a binder and bulking agent. This versatile excipient is suited for various dosage forms, including capsules, lozenges, and tablets.

Kollicoat® Protect is a versatile polyvinyl alcohol-polyethylene glycol copolymer designed for pharmaceutical and nutraceutical applications. Serving as a binder, emulsifying agent, film coating agent, and more, it excels in drug delivery and care solutions. This powder, utilized in oral, topical, and transdermal applications, stands out in pharmaceutical manufacturing as an excipient and coating. With its matrix-forming and taste-masking capabilities, Kollicoat® Protect ensures efficient and reliable performance. Its multifunctional nature extends to being a moisture barrier coating, enhancing its value in healthcare.

Kollidon® 90 F is a versatile polyvinylpyrrolidone (PVP) known for its role as a binder and stabilizer in pharmaceuticals and nutraceuticals. In powder form, it excels in healthcare and pharma applications, particularly in drug delivery and care solutions, both oral and topical. With a strong presence in pharmaceutical technologies, Kollidon® 90 F offers reliable performance, making it a preferred choice for formulators seeking effective binding and stabilizing capabilities

Cargill Pharm 12011 is a pregelatinized corn starch in the form of a white, free-flowing powder. This product is a binder compatible with most excipients and drugs. It is used in solid dosage formulations as a diluent/binder in direct compression and wet and dry granulation, as well as a diluent in capsule and powder formulations.

Cargill Pharm 12011 NGM is a pregelatinized corn starch in the form of a white, free-flowing powder derived from non-GM (NGM) maize. This product is used in solid dosage formulations as a diluent/binder in direct compression and wet and dry granulation, as well as a diluent in capsule and powder formulations.

Kollidon® VA 64 is a white or slightly yellowish, free-flowing powder with a faint characteristic odor and practically no taste. It readily dissolves in all hydrophilic solvents. Solutions of more than 10 % concentration can be prepared in water, ethanol, isopropanol, methylene chloride, glycerol and propylene glycol. It is less soluble in ether, cyclic, aliphatic and alicyclic hydrocarbons.

Kollicoat® SR 30 D is an aqueous dispersion with a solids content of 30%. The low viscosity product has a weak characteristic odor and a milky white or slightly yellowish appearance. The dispersion consists of about 27% polyvinyl acetate, 2.7% povidone and 0.3% sodium lauryl sulfate. Kollicoat® SR 30 D is miscible with water in any ratio while retaining its milky-white appearance. Mixing the product with ethanol or isopropyl alcohol in a 1:5 ratio produces a slightly turbid and somewhat viscous solution, a solution in acetone is more turbid. On addition of further organic solvents the polymer precipitates out but then dissolves when further solvent is added. It is insoluble in dilute alkaline or acidic solutions.

Kollicoat® IR is a white to faintly yellow free-flowing powder. The polymer consists of 75% polyvinyl alcohol units and 25% polyethylene glycol units. The product also contains approx. 0.3% colloidal anhydrous silica to improve its flow properties. As a result of its structure, the polymer dissolves very readily in acidic, neutral and alkaline aqueous media.

Kollitab™ DC 87 L is an almost white, odorless, and free-flowing powder. It is a coprocessed excipient based on lactose monohydrate (87%), crospovidone (9%), Kollicoat® IR (3%) and sodium stearyl fumarate (1%).

ADM Dextrose Monohydrate is produced through the enzymatic hydrolysis of starch, followed by purification, concentration, crystallization, and drying. It is a white calibrated powder with a refreshing sweet taste and bland odor, complying with EU and manufacturing country directives and regulations on foods and food ingredients, considered Non GMO. Dextrose, also known as glucose, is a simple sugar derived from various botanical sources like corn, wheat, fruits, and honey. It is widely used in a variety of products, including pharmaceutical applications, owing to its versatile functionality and benefits beyond sweetness.

ADM PharmaPlus Native Corn Starch 102 is a food-grade, native maize starch that appears as a fine, matte, white to slightly yellowish powder with a neutral odor and taste. This non-GMO product meets the requirements of the European Pharmacopeia (Ph.Eur.) and is Kosher and Halal certified.

T-Det® PEG 4000 F is a water-soluble polymer made from ethylene oxide. It has a wide range of applications as a humectant and viscosity modifier in the cosmetic and personal care industries, a mold release agent and lubricant in the rubber industry, and a binder and dry lubricant for pill and tablet manufacture in the pharmaceutical industry.

MASCEROL™ Glycerine 99.7 USP, non-GMO is highly refined with a minimum glycerol content of 99,7%. MASCEROL™ Refined Glycerine is used as a base ingredient in personal care preparations. It provides moisturizing properties and improves skin permeability. It is a gentle ingredient for anti-aging and anti-irritant cosmetics, found in skin & hair care applications, shaving cream, soaps & water-based lubricants. MASCEROL™ Refined Glycerine is used as an excipient in pharmaceutical production and preparations for improving smoothness, providing lubrication, and because of its humectant characteristics. It is found in allergen immunotherapies, cough syrups, tinctures, elixirs & expectorants. It is a tablet-holding agent and a key ingredient in soft gelatin capsules. In food as well as beverage applications MASCEROL™ serves as a humectant or wetting agent, solvent, sweetener or sugar substitute (approx. 60 % as sweet as sucrose), thickening agent, or filler.

MASCEROL™ Glycerine 99.7 USP, non-GMO, RSPO MB is highly refined with a minimum glycerol content of 99.7%. MASCEROL™ Refined Glycerine is used as a base ingredient in personal care preparations. It provides moisturizing properties and improves skin permeability. It is a gentle ingredient for anti-aging and anti-irritant cosmetics found in skin and hair care applications, shaving cream, soaps, and water-based lubricants. MASCEROL™ Refined Glycerine is used as an excipient in pharmaceutical production and preparations for improving smoothness, providing lubrication, and because of its humectant characteristics. It is also found in allergen immunotherapies, cough syrups, tinctures, elixirs, and expectorants. It is a tablet-holding agent and a key ingredient in soft gelatin capsules. In food as well as beverage applications, MASCEROL™ serves as a humectant or wetting agent, solvent, sweetener, or sugar substitute (approximately 60% as sweet as sucrose), thickening agent, or filler.

CERELOSE® Coarse Dextrose NF - 020350 is a coarse monohydrate dextrose product designed for applications requiring a unique coarser particle size profile, rounded and porous particle shape. This free-flowing material is manufactured according to IPEC cGMPs and tested for compliance with Dextrose Excipient NF standards. It can be used as an effective bulking agent in tablets, capsules, and other solid dosage forms to increase their volume and improve their handling properties besides having good compression ability. It meets the requirements of USP/ NF.

SORBOGEM® 712 Crystalline Sorbitol NF/FCC - 261054 is a white crystalline Sorbitol powder. It is an excellent excipient and diluent for effervescent and chewable tablets, and sachets. Its characteristics include free-flowing, non-browning, and non-cariogenic. It is also very soluble and has very good palatability. The sugar-free SORBOGEM® 712 is 60% sweet as sucrose and brings a pleasant cooling effect. It meets the requirements of USP/ NF.

UNI-PURE® F - 03451006 is a native corn starch. It is extra-white and free-flowing with not more than 15% moisture. It can be used as a Filler/Disintegrant for both hard-shell capsules and tablet dosage forms. When cooked in an aqueous system, it develops viscosity and sets to a firm gel upon cooling. The multi-compendial UNI-PURE® F meets the requirements of USP/NF, Ph. Eur., and JPE Pharmacopeias.

UNIDEX® Agglomerated Dextrose - 020540 is an agglomerated dextrose monohydrate product with maltodextrin. UNIDEX® has a very uniform coarse particle size profile and provides a range of functional benefits in Pharma tableting. It is very compressible to be used as a binder for direct compression, helping the tablet to remain intact during handling and transportation. It can also be used as an effective bulking agent, making it easier to handle the tablet during the manufacturing process. It has excellent flowability, reducing the risk of sticking and clogging during the tableting process.

SORBOGEM® 834 Crystalline Sorbitol NF/FCC - 261052 is a white crystalline Sorbitol powder. It is an excellent excipient and diluent for effervescent and chewable tablets, and sachets. SORBOGEM® 834 is used when a more uniform particle size distribution is required. Its characteristics include free-flowing, non-browning, and non-cariogenic. It is also very soluble and has very good palatability. The sugar-free SORBOGEM® 834 is 60% sweet as sucrose and brings a pleasant cooling effect. It meets the requirements of USP/ NF.

PURITY® 21T - 04730300 is a native starch derived from tapioca. It is extra white, free-flowing for use as a filler and disintegrant in a broad range of pharmaceutical applications. It develops viscosity as it is cooked in an aqueous system. Upon cooling, it will be set to a gel-like consistency. Its moisture is not more than 15%. It meets the requirements of USP/ NF.

Pharm-Rx Povidone, also known as polyvinylpyrrolidone copolymer, serves as a binder within pharmaceuticals and nutraceuticals. Operating in over-the-counter (OTC) capacities, it falls under binders and disintegrants within excipients. Povidone is commonly used in various formulations for its binding properties in pharmaceuticals.

Pharm-Rx Microcrystalline Cellulose (MCC 102) is a binder for pharma and nutraceuticals. Ingredient list includes microcrystalline cellulose.

Pharm-Rx Microcrystalline Cellulose (MCC 101) is a binder ingredient for pharma and nutraceuticals. Made of microcrystalline cellulose, it enhances product formulation.

CEAMPHARMA® is a plant based alternative to gelatin used as gelling, texturizing, heat resistance or viscosity agent in a wide range of nutraceutical applications. In syrup applications, it is used as a suspension and viscosity agent in liquid pharmaceutical formats.

Microcare™ 350GMP is a ultrafine #1 prime yellow carnauba wax for use as a coating and binding excipient in pharmaceutical and nutraceutical products.

METOLOSE® SM 1500 consists of methyl cellulose (USP, JP, EP) and three substitution types of hydroxypropyl methyl cellulose (hypromellose USP, JP, EP) each available in several grades differing in viscosity.

METOLOSE® 65SH-1500 consists of methyl cellulose (USP, JP, EP) and three substitution types of hydroxypropyl methyl cellulose (hypromellose USP, JP, EP) each available in several grades differing in viscosity. METOLOSE® 65SH-1500 provides a variety of functions such as water retention, protective colloid, surface activity, sustained release. It is a non-ionic compound resistant to salting out and stable over a wide pH-range. Typical applications of METOLOSE® 65SH-1500 are binder for solid dosage forms such as tablets and granules or thickener for liquid applications.

Capsules prepared from hypromellose have advantages in comparison with gelatin based capsules. Hypromellose capsules show a better moisture stability and are suitable for vegetarian/vegan patients. Low viscosity hypromellose products like METOLOSE 65SH-5 is suitable for capsule manufacturing.

METOLOSE® SM 15 consists of methyl cellulose (USP, JP, EP) and three substitution types of hydroxypropyl methyl cellulose (hypromellose USP, JP, EP) each available in several grades differing in viscosity.

METOLOSE® SM 4 consists of methyl cellulose (USP, JP, EP) and three substitution types of hydroxypropyl methyl cellulose (hypromellose USP, JP, EP) each available in several grades differing in viscosity.

METOLOSE® SM 400 consists of methyl cellulose (USP, JP, EP) and three substitution types of hydroxypropyl methyl cellulose (hypromellose USP, JP, EP) each available in several grades differing in viscosity.