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Products in Healthcare & Pharma: Orally Disintegrating Tablets (ODTs)
52 Products found in Healthcare & Pharma
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Roquette
MICROCEL® MC-102 Microcrystalline Cellulose - Pharma
Chemical Name:
Cellulose, Microcrystalline
CAS Number:
9004-34-6
Dosage Form:
Stick, Powder & Powder Blends, Tablets, Granules, Capsules, Pellets, Sachets, Orally Disintegrating Tablets (ODTs)
Labeling Claims:
Vegan, TSE-free, BSE-free, Pesticide-free, Halal, Kosher
Certifications & Compliance:
Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9001, United States Pharmacopeia (USP), Halal, Kosher, FDA IID
Manufacturing Technology:
Direct Compression
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
Roquette
StarLac® Lactose Monohydrate & Maize Starch Compound
Chemical Name:
Corn Starch, Lactose Monohydrate
Dosage Form:
Granules, Capsules, Pellets, Orally Disintegrating Tablets (ODTs), Powder & Powder Blends, Tablets
Certifications & Compliance:
ISO 9001, United States Pharmacopeia (USP), Japan Pharmacopeia (JP), National Formulary (NF), European Pharmacopeia (Ph. Eur.)
Manufacturing Technology:
Direct Compression, Dry Granulation
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.
Roquette
POLYSORB® 85/70/00
Ingredient Name:
Sorbitol
Chemical Name:
D-Glucitol
CAS Number:
50-70-4
Dosage Form:
Orally Disintegrating Tablets (ODTs), Capsules, Orally Disintegrating Films (ODFs), Soft Gels
POLYSORB® 85/70/00 Partially dehydrated sorbitol liquid is a plasticizer in soft capsules and orally dissolving films. It can be used in pharmaceutical dosage forms.POLYSORB® 85/70/00 is an aqueous solution of D-sorbitol and 1.4- sorbitans that has been developed by Roquette as a plasticizer for soft gelatine capsule applications. The advantage of this product in soft gels relates to its remarkable compatibility with gelatin that ensures no migration over time thereby preventing any defects like graining when crystallizing plasticizers are used or leaching phenomena either into the filler media or at the surface of the soft gel.
Roquette
NUTRIOSE® FM06 Dextrin - Pharma
Ingredient Name:
Dextrin
Chemical Name:
Dextrin
CAS Number:
9004-53-9
Dosage Form:
Sachets, Stick, Granules, Films, Lozenges, Orally Disintegrating Tablets (ODTs), Tablets, Capsules, Orally Disintegrating Films (ODFs), Pellets, Syrups, Suspension, Powder & Powder Blends
Labeling Claims:
BSE-free, Non-Hazardous, Non-GMO, Halal, Vegan, Melamine-free, Kosher, TSE-free, Gluten-free
NUTRIOSE® FM06 Dextrin can be used to add dietary fiber to capsules, films, granules, lozenges and other pharmaceutical applications. Benefits BSE-free Gluten-free Halal and Kosher certified Melamine-free Non-GMO Non-Hazardous TSE-free Vegan Features Chemical stability Easy dispersability
Roquette
MICROCEL® MC-101 Microcrystalline Cellulose - Pharma
Chemical Name:
Cellulose, Microcrystalline
CAS Number:
9004-34-6
Dosage Form:
Stick, Powder & Powder Blends, Tablets, Granules, Capsules, Pellets, Sachets, Orally Disintegrating Tablets (ODTs)
Labeling Claims:
Vegan, TSE-free, BSE-free, Pesticide-free, Halal, Kosher
Certifications & Compliance:
Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9001, United States Pharmacopeia (USP), Halal, Kosher, FDA IID
Manufacturing Technology:
Direct Compression, Wet Granulation
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
Roquette
GLYCOLYS® Low Solvent Sodium Starch Glycolate - Pharma
Chemical Name:
Sodium Carboxymethyl Starch
CAS Number:
9063-38-1
Functions:
Disintegrant
Manufacturing Technology:
Granulation
Labeling Claims:
BSE-free, Halal, Vegan, Kosher, TSE-free
Certifications & Compliance:
FSSC 22000, National Formulary (NF), FDA IID, United States Pharmacopeia (USP), Halal, Japan Pharmacopeia (JP), Canadian Environmental Protection Act (CEPA), FSSAI, ISO 9001, European Pharmacopeia (Ph. Eur.), Kosher
GLYCOLYS® Low Solvent Sodium Starch Glycolate is a superdisintegrant for pharmaceutical and nutraceutical swallowable tablets, orally dispersible tablets and hard capsules. Features Different grades designed to meet specific needs: Withstanding high shear granulation Acidic conditions Low organic solvent content
Roquette
PEARLITOL® Flash Mannitol - Pharma
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets
Labeling Claims:
BSE-free, Melamine-free, Halal, Non-GMO, Kosher, Vegan, Non-Hazardous, TSE-free
Certifications & Compliance:
ISO 9001, United States Pharmacopeia (USP), GMP, FDA Compliant, EXCiPACT, Halal, Kosher, ISO 50001, Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.)
Manufacturing Technology:
Direct Compression
PEARLITOL® Flash is used in nutraceutical and pharma oral dosage forms as a filler/binder for orally dispersable tablets. Applications Fast disintegrating tablets Orally dispersible tablets Benefits Excipient functional properties Disintegrant benefit Simplifies tablet formulation Features Compound of mannitol and starch adapted to direct compression formulation Excellent chemical inertness Consistent rapid disintegration under any compression force
Roquette
SOLUTAB® A Croscarmellose Sodium - Pharma
Chemical Name:
Croscarmellose Sodium
CAS Number:
74811-65-7
Functions:
Disintegrant
Manufacturing Technology:
Wet Granulation, Direct Compression
Labeling Claims:
BSE-free, Halal, Vegan, Kosher, TSE-free
Certifications & Compliance:
FSSC 22000, National Formulary (NF), FDA IID, United States Pharmacopeia (USP), Halal, Japan Pharmacopeia (JP), FSSAI, ISO 9001, European Pharmacopeia (Ph. Eur.), Kosher
SOLUTAB® Croscarmellose sodium is used in pharmaceutical and nutraceutical applications as a superdisintegrant for various oral dosage forms. Applications Swallowable tablets Orally dispersible tablets Hard capsules Blends Granules Pellets premix Benefit Efficient disintegration at low use level Features Crosslinked carboxymethyl cellulose sodium Three grades are available Disintegration performance is obtained through the wicking and swelling capacity that can be maximized via the selection of its origin (wood or cotton) Can be adapted to wet and dry granulation or direct compression processes
Roquette
KLEPTOSE® HPB Oral Grade Hydroxypropyl Betadex Cyclodextrin - Pharma
Chemical Name:
(2-Hydroxypropyl)-β-cyclodextrin
CAS Number:
128446-35-5
Dosage Form:
Granules, Injectables, Creams, Lozenges, Films, Syrups, Suspension, Tablets, Capsules, Pellets, Orally Disintegrating Tablets (ODTs), Powder & Powder Blends
Labeling Claims:
BSE-free, Halal, Kosher, Acrylamide-free, Vegan, Non-GMO, TSE-free
Certifications & Compliance:
GMP, FSSAI, Halal, Kosher, ISO 9001, FSSC 22000, United States Pharmacopeia (USP), EXCiPACT, FDA IID, European Pharmacopeia (Ph. Eur.)
KLEPTOSE® HPB Oral Grade is a solubilizer and stabilizer for pharmaceutical and nutraceutical oral dosage applications. Applications Swallowable, chewable and effervescent tablets Lozenges Hard and soft capsules Orally dissolving films Blends Granules Pellets premix Medicated confectionary Syrups Suspensions Liquids Cream Paste Semi-solids Benefits Improves the solubility of poorly soluble compounds Can be used for taste masking of bitter or unpleasant active ingredients
Roquette
Roquette POWDERED NF CORN STARCH
Chemical Name:
Corn Starch
Functions:
Filler, Disintegrant, Binder
Certifications & Compliance:
European Pharmacopeia (Ph. Eur.), National Formulary (NF), Japan Pharmacopeia (JP), Kosher, Halal, FDA IID, ISO 9001, United States Pharmacopeia (USP)
Labeling Claims:
Halal, Kosher
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
Roquette
PEARLITOL® 300 DC Mannitol - Pharma
Chemical Name:
D-mannitol
CAS Number:
69-65-8
Functions:
Binder, Filler
Dosage Form:
Orally Disintegrating Tablets (ODTs), Granules, Capsules, Tablets, Powder & Powder Blends
Labeling Claims:
Non-Carcinogenic, Vegan, Kosher, Halal, Melamine-free, BSE-free, Acrylamide-free, TSE-free, Sugar-free, Non-GMO
Certifications & Compliance:
FDA IID, Chinese Pharmacopeia (ChP), Canadian Environmental Protection Act (CEPA), FSSAI, EXCiPACT, ISO 9001, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), Japan Pharmacopeia (JP), Halal, Kosher, FSSC 22000, GMP
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, D-(-)-Mannitol, Manicol, Manitol
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
Roquette
NEOSORB® P 300 C Sorbitol - Pharma
Chemical Name:
D-Glucitol
Functions:
Binder, Filler
Certifications & Compliance:
United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia (JP), Canadian Environmental Protection Act (CEPA)
Labeling Claims:
Sugar-free, Non-Carcinogenic
Synonyms:
D-Sorbitol, D-Sorbol, Diakarmon, G-ol, Glc-ol, Glucarine, Karion, Multitol, Sionit, Sionite, Sorbilande
NEOSORB® Sorbitol pharma is used in pharmaceutical and nutraceutical formulations as a filler, filler/binder and bulk sweetener in various oral dosage applications, and as a plasticizing agent well-adapted to starches in coating/film forming applications. Applications Swallowable, orally dispersible, chewable and effervescent tablets Lozenges Blends Granules Pellets premix Medicated confectionery Features Excellent tableting properties Great organoleptic, non-cariogenic and sugar-free properties Suitable for use in formulations addressing pediatric and diabetic patient populations
Roquette
PEARLITOL® 100 SD Mannitol - Pharma
Chemical Name:
D-mannitol
Functions:
Binder, Filler
CAS Number:
69-65-8
Dosage Form:
Orally Disintegrating Tablets (ODTs), Capsules, Tablets
Labeling Claims:
Vegan, BSE-free, Kosher, Acrylamide-free, Halal, TSE-free, Non-GMO
Certifications & Compliance:
United States Pharmacopeia (USP), FDA IID, Japan Pharmacopeia (JP), Chinese Pharmacopeia (ChP), EXCiPACT, ISO 9001, Halal, European Pharmacopeia (Ph. Eur.), Kosher, GMP
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, D-(-)-Mannitol, Manicol, Manitol
PEARLITOL® Mannitol pharma range is used in pharmaceutical and nutraceutical formulations as a filler, filler/binder and bulk sweetener in oral dosage form 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
PEARLITOL® 200 GT-EXP
Chemical Name:
Mannitol
CAS Number:
87-78-5
Functions:
Filler, Sweetener, Binder
Dosage Form:
Pellets, Lozenges, Orally Disintegrating Tablets (ODTs), Powder & Powder Blends, Tablets, Other Dosage Forms
Labeling Claims:
Non-Cariogenic
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, Manicol, Manitol
PEARLITOL® 200 GT-EXP is a direct compression excipient specifically formulated to enhance the manufacturing process of tablets. This exceptional excipient is designed to address key challenges such as capping, while improving flowability and tabletability. PEARLITOL® 200 GT-EXP is a granulated form of mannitol known for its outstanding physical and chemical stability. With its high API compatibility and non-hygroscopic nature, it ensures consistent quality and performance in pharmaceutical formulations. As a non-cariogenic and non-acidogenic sugar-free sweetener, it is suitable for various patient populations, including pediatric and diabetic individuals. PEARLITOL® 200 GT-EXP finds application in a wide range of dosage forms, including tablets (lozenges, swallowable, orally dispersible, chewable, and effervescent) as well as powder blends (sachets, oral stick packs, and hard gelatin capsules).
Roquette
PEARLITOL® 25 C Mannitol - Pharma
Chemical Name:
D-mannitol
CAS Number:
69-65-8
Functions:
Filler, Sweetener, Binder
Dosage Form:
Granules, Tablets, Pellets, Lozenges, Orally Disintegrating Tablets (ODTs), Powder & Powder Blends
Labeling Claims:
Vegan, Sugar-free, Kosher, TSE-free, Melamine-free, Non-Hazardous, Non-Carcinogenic, BSE-free, Halal
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, D-(-)-Mannitol, Manicol, Manitol
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
Roquette
Roquette 400L-NF Corn Starch - Pharma
Chemical Name:
Corn Starch, Modified
Functions:
Binder, Filler, Disintegrant
Certifications & Compliance:
Kosher, Halal, United States Pharmacopeia (USP), Japan Pharmacopeia (JP), FDA IID, ISO 9001, FSSAI, European Pharmacopeia (Ph. Eur.), National Formulary (NF), FSSC 22000, DMF Type II
Labeling Claims:
Melamine-free, BSE-free, TSE-free, Kosher, Vegan, Halal, Acrylamide-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
Roquette
PEARLITOL® 200 SD Mannitol - Pharma
Chemical Name:
D-mannitol
CAS Number:
69-65-8
Functions:
Binder, Filler
Dosage Form:
Orally Disintegrating Tablets (ODTs), Granules, Capsules, Tablets, Powder & Powder Blends
Labeling Claims:
Non-Carcinogenic, Vegan, Kosher, Halal, Melamine-free, BSE-free, Acrylamide-free, TSE-free, Sugar-free, Non-GMO
Certifications & Compliance:
FDA IID, Chinese Pharmacopeia (ChP), FSSAI, EXCiPACT, ISO 9001, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), Japan Pharmacopeia (JP), Halal, Kosher, FSSC 22000, GMP
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, D-(-)-Mannitol, Manicol, Manitol
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
PEARLITOL® 160 C - Mannitol
Chemical Name:
D-mannitol
Functions:
Binder, Sweetener, Filler
CAS Number:
69-65-8
Dosage Form:
Orally Disintegrating Tablets (ODTs), Powder & Powder Blends, Tablets, Capsules, Granules
Labeling Claims:
Non-Cariogenic, Sugar-free
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, D-(-)-Mannitol, Manicol, Manitol
PEARLITOL® 160 C - Mannitol is a versatile excipient for nutraceutical and pharmaceutical oral dosage applications. Suitable for use in capsules, granules, orally disintegrating tablets (ODTs), powders, and tablets, PEARLITOL® 160 C supports direct compression manufacturing. It boasts high physical and chemical stability, and it is non-hygroscopic, ensuring long-lasting quality. Ideal for healthcare and pharma , this excipient enhances drug delivery and care solutions with its excellent performance and stability.
Roquette
PEARLITOL® 50 C Mannitol - Pharma
Chemical Name:
Mannitol
Functions:
Filler, Sweetener, Binder
CAS Number:
87-78-5
Dosage Form:
Capsules, Granules, Tablets, Orally Disintegrating Tablets (ODTs), Powder & Powder Blends
Labeling Claims:
Vegan, Sugar-free, Kosher, Melamine-free, Acrylamide-free, Non-Carcinogenic, Halal
Synonyms:
1,2,3,4,5,6-Hexanehexol, Cordycepic Acid, Manicol, Manitol
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
Atomgrid
Atomgrid Paracetamol USP (Acetaminophen USP )
Chemical Name:
Acetaminophen
CAS Number:
103-90-2
Dosage Form:
Orally Disintegrating Tablets (ODTs)
Certifications & Compliance:
United States Pharmacopeia (USP)
Atomgrid Paracetamol USP (Acetaminophen USP ) is a water-soluble powder used as an API intermediate in pharmaceutical and nutraceutical applications. It meets the standards set by the United States Pharmacopeia (USP) and is specifically formulated for orally disintegrating tablets (ODTs), ensuring effective dosage and rapid dissolution
Shin-Etsu Pharma, Nutra and Food
L-HPC NBD-022
Chemical Name:
Low-Substituted Hydroxypropyl Cellulose
Functions:
Binder, Disintegrant
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets, Pellets
Labeling Claims:
Non-GMO, TSE-free, Allergen-free, Kosher, Solvent-free, BSE-free
Certifications & Compliance:
National Formulary (NF), United States Pharmacopeia (USP), DMF Type IV, European Pharmacopeia (Ph. Eur.), The Food Allergen Labeling & Consumer Protection Act of 2004 (FALCPA), GMP, Japan Pharmacopeia (JP), Kosher
L-HPC (low-substituted hydroxypropyl cellulose NF, JP, EP) This dual functioning excipient acts as both a disintegrant and binder. It is not the same as HPC. L-HPC is insoluble in water. It is an effective disintegrant due to its swelling action in water. Because is has good compressibility, it functions as a dry binder.NBD Grades:Better flowability because of the non-fibrous particle shapeBetter compressibilityBetter tasteEnhanced stability because it is non-ionic and has low water activityIt is peroxide free and provides excellent compatibility for oxygen sensitive APIsA variety of grades are available depending on the application. L-HPC NBD-022 is suitable for direct compression and ODTs.
Shin-Etsu Pharma, Nutra and Food
SmartEx® QD-50
Functions:
Filler, Disintegrant, Binder
Dosage Form:
Orally Disintegrating Tablets (ODTs)
Certifications & Compliance:
DMF Type IV, Japan Pharmacopeia (JP)
SmartEx® is a co-processed excipient which consists of L-HPC, D-mannitol and fully hydrolyzed polyvinyl alcohol (PVA) and it specially designed for orally disintegration tablets (ODTs) and also immediate release tablet formulation by direct compression. All the excipients are widely used in pharmaceutical industry. One of the main advantage over other co-processed excipients is that SmartEx® contains L-HPC and therefore gives excellent stability.
Shin-Etsu Pharma, Nutra and Food
SmartEx® QD-100
Functions:
Filler, Disintegrant, Binder
Dosage Form:
Orally Disintegrating Tablets (ODTs)
Certifications & Compliance:
DMF Type IV, Japan Pharmacopeia (JP)
SmartEx® is a co-processed excipient which consists of L-HPC, D-mannitol and fully hydrolyzed polyvinyl alcohol (PVA) and it specially designed for orally disintegration tablets (ODTs) and also immediate release tablet formulation by direct compression. All the excipients are widely used in pharmaceutical industry. One of the main advantage over other co-processed excipients is that SmartEx® contains L-HPC and therefore gives excellent stability.
Biogrund
CompactCel® DIS
Functions:
Disintegrant
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets, Capsules
Labeling Claims:
Palm Oil-free, Titanium dioxide-free, Silica-free, Synthetic Polymers-free, Magnesium Stearate-free, Clean Label, Silicon dioxide-free, Organic, Talc-free
Certifications & Compliance:
United States Pharmacopeia (USP), EXCiPACT, European Pharmacopeia (Ph. Eur.), Organic Certified, USDA Organic, ISO 9001
CompactCel® DIS is a natural/organic super-disintegrant which enables a rapid break-up of solid dosage forms when they come into contact with moisture. The super-disintegrant premix is formulated with natrual ingredients which complies with current Clean Label Standards. It provides an alternative to synthetic super-disintegrants, such as crosslinked polymers, crosscarmellose sodium or sodium starch glycolate. CompactCel® DIS helps in the fast breakdown of the solid dosage form so that the active ingredient becomes bioavailable faster and is readily absorbed. It can be also used in the formulation of oral disintegrating tablets (ODT) or chewing tablets.
PHARMATRANS SANAQ AG
IBUPROFEN DC-100
Chemical Name:
Ibuprofen
CAS Number:
15687-27-1
Certifications & Compliance:
European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP)
Dosage Form:
Tablets, Orally Disintegrating Tablets (ODTs)
Labeling Claims:
TSE-free, BSE-free
Synonyms:
(+-)-Ibuprofen, (±)-2-(p-isobutylphenyl)propionic acid, (±)-ibuprofen, (±)-p-isobutylhydratropic acid, (±)-α-methyl-4-(2-methylpropyl)benzeneacetic acid, (4-isobutylphenyl)-α-methylacetic acid, (RS)-ibuprofen, 2-(4-isobutylphenyl)propanoic acid, 4-Isobutylhydratropic acid, alpha-(4-Isobutylphenyl)Propionic Acid, alpha-(P-Isobutylphenyl)Propionic Acid, p-Isobutyl-2-phenylpropionic acid, p-Isobutylhydratropic acid, α-(4-isobutylphenyl)propionic acid, α-(p-isobutylphenyl)propionic acid
Ibuprofen DC 100 are spherically shaped particles consisting of 100 % Ibuprofen drug substance.Due to its shape and surface structure Ibuprofen DC 100 provides unique product characteristics offering a wide range of applications.
PHARMATRANS SANAQ AG
DICOM SANAQ® SR 300
Chemical Name:
Silicon Dioxide, Colloidal , Low-Substituted Hydroxypropyl Cellulose, Ethylcellulose, Magnesium Stearate, Hydroxypropyl Methylcellulose, Silicon Dioxide, Cellulose, Microcrystalline, Talc
Functions:
Matrix Forming Agent
Certifications & Compliance:
European Pharmacopeia (Ph. Eur.), National Formulary (NF), Japan Pharmacopeia (JP), United States Pharmacopeia (USP)
Dosage Form:
Tablets, Orally Disintegrating Tablets (ODTs)
Off white free flowing granules.
PHARMATRANS SANAQ AG
DICOM SANAQ® LS 004
Chemical Name:
Starch, Lactose, Anhydrous
Functions:
Binder, Disintegrant
Manufacturing Technology:
Direct Compression
Certifications & Compliance:
National Formulary (NF), Japan Pharmacopeia (JP), GMP, ISO 9001, United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.)
DICOM SANAQ® LS 004 have average particle size of 300 - 550 microns. It is a combination of Lactose Monohydrate and Starch (maize). Lactose is water loving and soluble in water, at high compression force it hampers disintegration. Starch has multifunction characters and act as binder as well as disintegrant. Starlose has optimized composition of these two ingredients.
PHARMATRANS SANAQ AG
DICOM SANAQ® ML 011
Chemical Name:
Lactose, Anhydrous, Cellulose, Microcrystalline
Functions:
Binder, Diluent
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets
Certifications & Compliance:
National Formulary (NF), United States Pharmacopeia (USP), GMP, Japan Pharmacopeia (JP), ISO 9001, European Pharmacopeia (Ph. Eur.)
Off white free flowing granules.
PHARMATRANS SANAQ AG
DICOM SANAQ® SP 205
Chemical Name:
Cellulose, Microcrystalline, Silicon Dioxide, Colloidal , Silicon Dioxide, Polyvinyl Pyrrolidone Copolymer
Functions:
Diluent
Manufacturing Technology:
Direct Compression
Certifications & Compliance:
GMP, ISO 9001, Japan Pharmacopeia (JP), United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.), National Formulary (NF)
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets
Off white free flowing granules.
PHARMATRANS SANAQ AG
DICOM SANAQ® SP 206
Chemical Name:
Silicon Dioxide, Colloidal , Polyvinyl Pyrrolidone Copolymer, Sodium Carboxymethyl Starch, Silicon Dioxide, Cellulose, Microcrystalline
Functions:
Diluent
Manufacturing Technology:
Direct Compression
Certifications & Compliance:
ISO 9001, European Pharmacopeia (Ph. Eur.), National Formulary (NF), GMP, Japan Pharmacopeia (JP), United States Pharmacopeia (USP)
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets
Off white free flowing granules.
PHARMATRANS SANAQ AG
DICOM SANAQ® SP 204
Chemical Name:
Starch, Pregelatinized, Sodium Carboxymethyl Starch, Magnesium Peroxide, Cellulose, Microcrystalline, Starch
Functions:
Binder, Diluent
Dosage Form:
Orally Disintegrating Tablets (ODTs), Tablets
Certifications & Compliance:
National Formulary (NF), United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.), GMP, Japan Pharmacopeia (JP), ISO 9001
Off white free flowing granules.
PHARMATRANS SANAQ AG
SSG SANAQ® Type A
Chemical Name:
Sodium Carboxymethyl Starch
CAS Number:
9063-38-1
Manufacturing Technology:
Direct Compression, Wet Granulation
Functions:
Disintegrant
Certifications & Compliance:
National Formulary (NF), United States Pharmacopeia (USP), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.)
Synonyms:
Carboxymethyl starch sodium salt, Sodium starch glycolate
SSG SANAQ® Type A is Blue color with iodine reagent
Fuji Health Science, Inc.
Fujicalin®
Functions:
Flow Promoter, Anti-Caking Agent, Compression Aid, Binder, Disintegrant
Dosage Form:
Orally Disintegrating Tablets (ODTs)
Certifications & Compliance:
United States Pharmacopeia (USP), DMF Type IV, GMP, Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.)
Fujicalin® is a dibasic calcium phosphate anhydrous designed to function as a direct compression excipient. It has exceptional flow and compression characteristics, while maintaining the ability for rapid disintegration. The key to Fujicalin®’s superior performance is the highly specialized and proprietary manufacturing process that yields a unique primary particle.
Freund
NONPAREIL® 108-200
Functions:
Filler, Controlled Release Agent
Dosage Form:
Granules, Orally Disintegrating Tablets (ODTs), Capsules, Tablets
Certifications & Compliance:
Japan Pharmacopeia (JP)
Nonpareil is perfect as a core for elaborate granule for pharmaceutical preparation with narrow particle size distribution and high sphericity.
Fuji Health Science, Inc.
F-MELT® Type F1
Functions:
Disintegrant
Manufacturing Technology:
Direct Compression
Certifications & Compliance:
Indian Pharmacopeia, Japan Pharmacopeia (JP), Chinese Pharmacopeia (ChP)
F-Melt® Type F1 is a proprietary co-spray dried excipient launched by Fuji in 2005. F-Melt® is designed not only for manufacturing orally disintegrating tablets (ODTs) and tablets that dissolve fast in the oral cavity without the need of water, but is also an excellent excipient for soft chewable tablets. It is suitable for manufacturing directly compressible ODTs simply by blending with active pharmaceutical ingredients (APIs) and lubricants. F-Melt® Type F1 is mainly used for dietary supplement applications.
GELPELL AG
GELPELL®
Functions:
Complexing Agent
Labeling Claims:
Preservative-free, Clean Label, Additive-free, Organic
Certifications & Compliance:
GMP, Organic Certified, ISO 22000
Dosage Form:
Orally Disintegrating Tablets (ODTs)
Gelpell® are also called nutrient pearls. This new, attractive dosage form is ideal for many valuable active substances and offers substantial advantages. The resulting Gelpell® look great, are round, 0.8mm to 2.0mm in size, easy to handle and they are comfortable to swallow. Exclusive to the Gelpell technology is the ability to produce transparent Gelpell®, which can not be achieved by other standard processes i.e. extrusion or layering on sugar cores.
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