Products in Fillers & Diluents: Granules

PEARLITOL® Mannitol pharma range is used as a filler and filler/binder. The PEARLITOL® range offers a unique blend of exceptional physical and chemical stability with no hygroscopicity. Using different texturizing technologies, we have designed a crystalline range of directly compressible PEARLITOL® with various particle sizes, allowing you to find the right product. With great organoleptic, non-cariogenic, and sugar-free properties. PEARLITOL® is suitable to be used in formulations addressing all types of patient populations, including paediatrics and diabetics.  PEARLITOL® can be used in various oral dosage forms in both pharmaceutical and nutraceutical applications, including swallowable tablets, orally dispersible tablets, chewable tablets, effervescent tablets, lozenges, blends, granules, pellet premixes, and medicated confectionary.

LYCATAB® PGS is used in pharmaceutical and nutraceutical applications as a binder for wet granulation. Features Natural pregelatinized maize starch resulting from a combination of the natural binding properties of pregels starches and a controlled manufacturing process Dispersible and partially soluble in cold water and ready for use High-stability reproducible binding properties during granulation and dissolution profile of actives in final forms Can be used in granules and swallowable forms

PEARLITOL® Mannitol is used in pharmaceutical and nutraceutical formulations as a filler, filler/binder and bulk sweetener in various oral dosage applications. Applications Swallowable, orally dispersible, chewable and effervescent tablets Lozenges Blends Granules Pellets premix Medicated confectionery Features Unique blend of exceptional physical and chemical stability and no hygroscopicity Directly compressible crystalline range with various particle sizes Great organoleptic, non-cariogenic and sugar-free properties Suitable for use in formulations addressing pediatric and diabetic patient populations

Roquette powdered NF corn starch is used in pharmaceutical and nutraceutical formulations as a disintegrant, filler and binder (once cooked). Applications Swallowable tablets Hard capsules Blends Granules Pellets premix

PEARLITOL® Mannitol pharma range is used in pharmaceutical and nutraceutical applications as a filler, filler/binder and bulk sweetener for various oral dosage forms. Applications Swallowable, orally dispersible, chewable and effervescent tablets, Lozenges Blends Granules Pellets premix Medicated confectionery Benefit Suitable for use in formulations addressing all types of patient populations, including pediatric and diabetic Features Directly compressible Unique blend of exceptional physical and chemical stability No hygroscopicity Organoleptic, non-cariogenic and sugar-free properties

TACKIDEX® Potato dextrins provide a variety of benefits to the manufacturer and consumer as both an excipient and a nutrient. They are white to yellow powders obtained from maize, tapioca, and potato starch by heat treatment. These are ingredients for clinical nutrition and nutraceuticals. Dextrins are starch polymers derived through solid-state heating from partially hydrolysed starch. Dextrinization is a classical starch processing technology that makes partial or complete solubility possible. As an excipient, dextrins are a binder, filler, stabilizer,  suspending agent, and viscosifier. As a nutrient, it is a carbohydrate and fiber source. TACKIDEX® can be used in various oral dosage forms in both pharmaceutical and nutraceutical applications, including swallowable tablets, chewable tablets, effervescent tablets, lozenges, hard capsules, soft capsules, coatings, orally dissolving films, blends, granules, pellet premix, medicated confectionary, syrups, suspensions, and liquids.

Roquette Pea Starch N735 is a versatile ingredient that serves as an anti-caking agent, binder, carbohydrate source, and texturizing agent. Available in powder form, this neutral-scented, white to off-white powder effortlessly enhances your formulations. It offers alcohol solubility and a neutral taste.

MICROCEL® Microcrystalline cellulose is used in pharmaceutical and nutraceutical applications as a filler/binder and fiber source in various oral dosage forms. Applications Swallowable tablets Hard capsules Blends Granules Pellets premix Features Available in a large range to meet different formulation, process and dosage form requirements Large surface area allows adsorption of particles or liquids and a certain capacity to act as a disintegrant Spray dried and offered from EXCiPACT (International Pharmaceutical Excipients Certification) certified plant

StarLac® Co-processed lactose starch is a filler/binder with strong disintegrant properties. The co-processing offers superior benefit compared to a blend of lactose and starch. It allows to improve the performance (hardness, friability, disintegration time) of your formulation. Specifically designed for direct compression applications, StarLac® is also an excellent filler/binder in dry granulation processes. StarLac® can be used in various oral dosage forms in pharmaceutical applications including granules, swallowable tablets, orally dispersible tablets and hard capsules.

NEOSORB® XTAB 300S is a directly compressible sorbitol powder that can be used for very hard, sugar-free tablets with high flavor load. Benefits Delivers a smooth, hard and uniform colored surface Provides a clean, cooling effect Does not produce acids or cause dental plaque or tooth decay Nutritional benefits (maintenance of tooth mineralization, tooth-friendly generic EU claims) recognized by European regulations Features Non-cariogenic Sugar-free

Roquette 400L-NF Corn Starch is an oxidized maize starch that can be used as a disintegrant filler and binder (once cooked) in a variety of nutraceutical and pharmaceutical dosage forms, including swallowable tablets, hard capsules, blends, granules and pellets premix. Benefits Acrylamide-free BSE-free Halal and Kosher certified Melamine-free TSE-free Vegan

PEARLITOL® Mannitol pharma range is used as a filler and filler/binder. The PEARLITOL® range offers a unique blend of exceptional physical and chemical stability and no hygroscopicity. Using different texturizing technologies we have designed a crystalline range of directly compressible PEARLITOL® with various particle size allowing you to find the right product. With great organoleptic, non-cariogenic and sugar-free properties PEARLITOL® is suitable to be used in formulation addressing all type of patient population including pediatric and diabetic. PEARLITOL® can be used in in various oral dosage forms in both pharmaceutical and nutraceutical applications including swallowable tablets, orally dispersible tablets, chewable tablets, effervescent tablets, lozenges, blends, granules, pellets premix and medicated confectionary

PEARLITOL® 25 C Mannitol is a filler and bulk sweetener that can be used for pharmaceutical oral dosage applications. Benefits BSE-free Halal and Kosher certified Melamine-free Non-carcinogenic Non-hazardous Sugar-free TSE-free Vegan Features High physical and chemical stability Cooling effect Non-cariogenic Low hygroscopicity

MICROCEL® Microcrystalline cellulose is used in both pharmaceutical and nutraceutical applications as a filler/binder and fiber source in various oral dosage forms. Applications Swallowable tablets Hard capsules Blends Granules Pellets premix Features Available in a large range to meet different formulation, process and dosage form requirements Large surface area allows adsorption of particles or liquids and a certain capacity to act as a disintegrant Spin flash-dried

PEARLITOL® Mannitol pharma range is used in pharmaceutical and nutraceutical formulations as a filler, filler/binder and bulk sweetener in various oral dosage applications. Applications Swallowable, orally dispersible, chewable and effervescent tablets Lozenges Blends Granules Pellets premix Medicated confectionery Features Unique blend of exceptional physical and chemical stability and no hygroscopicity Directly compressible crystalline range with various particle sizes Great organoleptic, non-cariogenic and sugar-free properties Suitable for use in formulations addressing pediatric and diabetic patient populations

Kollidon® SR, a synthetic ingredient, excels in pharmaceuticals and nutraceuticals as a versatile solution. Serving as a controlled release agent, filler, film former, matrix forming agent, solvent, sustained release agent, and viscosity modifier, it proves indispensable in diverse applications. Found in powder form, it is tailored for healthcare and pharmaceutical needs, specializing in oral and topical drug delivery and care solutions. This innovative technology redefines pharmaceutical formulations, ensuring optimal performance in controlled and sustained release scenarios.

NONPAREIL®-101 24-32 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.

NONPAREIL®-105 150 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.

NONPAREIL®-103 32-42 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.

NONPAREIL®-103 24-32 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.

Dilactose F (Fine) is a Japanese Pharmacopeia, Lactose Hydrate (granulated powder) developed by our unique fluid bed granulation method. It is useful as an excipient for directly compression. F (Fine) is small particle size grade Dilactose. In comparison with the existing grades, both formability and disintegration have been improved.

Dilactose R is a Japanese Pharmacopeia, Lactose Hydrate (granulated powder) developed by our unique fluid bed granulation method. It is useful as an excipient for directly compression. F (Fine) is small particle size grade Dilactose. In comparison with the existing grades, both formability and disintegration have been improved.

NONPAREIL®-103 20-24 is a spherical granule consists of purified sucrose.

NONPAREIL®-101 20-24 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.

Shanghai Qifuqing Material Technology PVPP-R is a cross-linked polymer that is polymerized from vinyl pyrrolidone monomer under specific conditions and is insoluble in water, strong acids, strong bases and general organic solvents.

Huangshan Bonsun Pharmaceuticals Crospovidone Food grade E1202 is a white or almost white free-flowing powder, no special odor, insoluble in water, acid, alkali and common solvents; it has strong swelling in water, does not form a gel after swelling, and has very good compatibility with polyphenols. , Carboxylic acid, tannin and small molecule substances complex. It is considered to be the preferred disintegrant for high-end tablets. It is especially suitable for the formulation of instant and chewable tablets. It is also widely used in food-grade products and beer and beverage industries.

NONPAREIL®-101 24-32 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.

Dilactose S is a Japanese Pharmacopeia, Lactose Hydrate (granulated powder) developed by our unique fluid bed granulation method. It is useful as an excipient for directly compression. F (Fine) is small particle size grade Dilactose. In comparison with the existing grades, both formability and disintegration have been improved.

Nonpareil is perfect as a core for elaborate granule for pharmaceutical preparation with narrow particle size distribution and high sphericity.

Nonpareil is perfect as a core for elaborate granule for pharmaceutical preparation with narrow particle size distribution and high sphericity.

Shanghai Qifuqing Material Technology PVPP-F is a cross-linked polymer that is polymerized from vinyl pyrrolidone monomer under specific conditions and is insoluble in water, strong acids, strong bases and general organic solvents.

Nonpareil is perfect as a core for elaborate granule for pharmaceutical preparation with narrow particle size distribution and high sphericity.

NONPAREIL®-105 50-83 is a spherical granule made from purified sucrose and starch.It is possible to calculate volume and surface dimension and it is easy to control film thickness in controlled-release drugs.Narrow particle size distribution When layering drugs, granules with sharp particle size distribution can be obtained.In addition, the thickness of film does not vary in the layering process and the speed of API release should be very stable.