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IFF Pharma Solutions

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91 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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POLYOX™ WSR - N12K NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N12K NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N12K NF Grade is an off-white powder with water-soluble properties. It's used as a binder and thickener in cleaning products and pharmaceuticals. Its applications include gels, osmotic pump tablets, and regular tablets, and it's manufactured using direct compression technology. Additionally, it serves as a controlled release agent.
POLYOX™ WSR - 205 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 205 NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 205 NF Grade characterized by its off-white color, is available in powder form. It serves as a binder and thickener in various industrial applications. Its water solubility makes it suitable for abuse deterrent tablets and capsules, gels, and osmotic pump tablets.
POLYOX™ WSR - N80 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - N80 NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Not Listed In California Proposition 65, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Clean Water Act (CWA) Certified, Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - N80 NF Grade is an off-white to white powder that is water soluble. It is used in dosage forms such as abuse deterrent tablets, capsules, and gels, providing essential properties for these pharmaceutical applications.
ETHOCEL™ Standard 7 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 7 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
  • Dosage Form:Tablets
  • Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, GMO-free, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), FDA 21 CFR 573.420, European Regulation 396/2005/EC, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
  • Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Tablet Coating, Granulation
ETHOCEL™ Standard 7 Premium Ethylcellulose White Powder has binding, controlled release, flexibility, and thermal stability benefits. It's soluble in organic solvents and ethanol. Used in direct compression, encapsulation, granulation, hot melt extrusion, and tablet coating. It functions as a controlled release agent, granulation aid, and taste masking agent.
ETHOCEL™ Standard 10 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 10 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
  • Dosage Form:Tablets
  • Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, GMO-free, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), FDA 21 CFR 573.420, European Regulation 396/2005/EC, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Halal, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
  • Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Tablet Coating, Granulation
ETHOCEL™ Standard 10 Premium Ethylcellulose characterized by its white color, serves as a stabilizer and thickener in cosmetic ingredients. Utilizing encapsulation, granulation, hot melt extrusion, and tablet coating technologies, it is available in a powdered physical form.
METHOCEL™ E50 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ E50 Premium LV HPMC
  • INCI Name:Methylcellulose
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Dosage Form:Tablets, Suspension
  • Ingredient Origin:Plant Origin
  • Labeling Claims:Phthalates-free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Animal Products-free, Allergen-free, Residual Solvent -Free, Halal, Hypoallergenic, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, VOC-free, TSE-free, Pareve, Perfluorooctanoic Acid-free, Aflatoxin-free, Endocrine Disruptor-free, Plant-Based, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, USP 232 Elemental Impurities Free, Mycotoxins-free, Kosher, Dye Free, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, APE-free, Odor-free, Pesticide-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, Not Listed In California Proposition 65, PFOS-free, BSE-free, Natural Latex Rubber-Free, Tributyl Tin Compounds-Free, Vegan, Low Odor
METHOCEL™ E50 Premium LV HPMC is a versatile ingredient suitable for various applications. In suspension dosage forms, it serves as a binder for ceramics, while its granulation and tablet coating manufacturing technologies make it adaptable for different production processes. With properties such as film formation, gelling, and mucoadhesion, it functions in pharmaceutical and nutraceutical applications, facilitating immediate release and solubilization when needed.
ETHOCEL™ Standard 100 FP Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 100 FP Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Granulation Aid, Binder, Taste Masker, Controlled Release Agent
  • Dosage Form:Tablets
  • Labeling Claims:Antibiotics-free, Endocrine Disruptor-free, Nitrosamines-free, Natural Latex Rubber-Free, Vegetarian, Dye Free, Kosher, Naturally Derived, Vegan, Zero Calorie, TSE-free, PVC-free, Colorants-free, Aluminum-free, Glycerin-free, Pesticide-free, 1,4-Dioxane-free, Sugar-free, PAH-free, Plant-Based, Irradiation-free, Monosodium Glutamate (MSG)-free, Phthalates-free, Perfluorooctanoic Acid-free, Palm Oil-free, CMR Substances-free, Mycotoxins-free, Dioxin-free, PHO (Partially Hydrogenated Oil)-Free, Triphenyl Tin Compounds-Free, PFAS-Free, Caffeine Free, Bisphenol A-free, Hormones-free, Aflatoxin-free, Preservative-free, Tributyl Tin Compounds-Free, APE-free, PFOS-free, VOC-free, BSE-free, Paraben-free, Halal, Formaldehyde-free, Organic, Sewage Sludge Free, Plasticizer-free
  • Certifications & Compliance:FDA 21 CFR 163, Japan Pharmacopeia (JP), Japan Chemical Substances Control Law (CSCL), Swiss Ordinance (SR 817.023.21), Canadian Environmental Protection Act (CEPA), FDA 21 CFR 573.420, European Regulation 396/2005/EC, Clean Air Act (CAA) Certified, FSSC 22000, FDA 21 CFR 172.868, Regulation (EU) No. 231/2012, ISO 9001, Majelis Ulama Indonesia Halal, WEEE Directive 2012/19/EU, FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, Directive 2023/915/EU, European Pharmacopeia (Ph. Eur.), Regulation (EC) No. 1333/2008, RoHS Compliant, United States Pharmacopeia (USP), FDA 21 CFR 73.1, Organic Certified, EC No.1907/2006, Indian Pharmacopeia, cGMP, FDA Food Safety Modernization Act (FSMA), CFDA Compliant (China), EuPIA Listed, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, Regulation (EU) No. 1169/2011, FDA 21 CFR 181.24, National Formulary (NF), RoHS 2 Compliant, Turkish RoHS Regulation, EXCiPACT, Generally Recognized As Safe (GRAS), FCC Compliant, Regulation (EU) No. 10/2011 (PIM), USDA Organic, FDA 21 CFR 73.1001, Directive 2009/48/EC, British Pharmacopeia (BP), Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), GMP
  • Manufacturing Technology:Hot Melt Extrusion, Encapsulation, Direct Compression, Tablet Coating, Granulation
ETHOCEL™ Standard 100 FP Premium Ethylcellulose a white powdered ethylcellulose variant, boasts benefits such as controlled release, excellent flexibility, and thermal stability. Its utility extends to cosmetic applications, where it functions as a stabilizer and thickener. Its manufacturing technology includes direct compression, encapsulation, granulation, and hot melt extrusion processes.
POLYOX™ WSR - 1105 NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR - 1105 NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Thickener, Flocculant, Viscosity Modifier, Binder, Lubricant, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR - 1105 NF Grade an off-white powder, serves as a binder and thickener in cleaning agents. It is available in powder form and is water-soluble, making it suitable for use in gels and osmotic pump tablets.
POLYOX™ WSR Coagulant LEO NF Grade banner
IFF Pharma SolutionsPOLYOX™ WSR Coagulant LEO NF Grade
  • Chemical Name:Polyethylene Oxide
  • CAS Number:25322-68-3
  • Functions:Lubricant (Internal), Film Former, Flocculant, Binder, Controlled Release Agent
  • Dosage Form:Tablets, Abuse Deterrent Tablets & Capsules, Osmotic Pump Tablet, Gels
  • Labeling Claims:Chlorine-free, Nitrosamines-free, Vegetarian, Heavy Metal-free, Kosher, Naturally Derived, Vegan, TSE-free, Diethylene Glycol-free, Allergen-free, Residual Solvent -Free, Plant-Based, Ethylene Glycol-free, Oxidatively Degradable, Animal Products-free, Dairy-free, Not Tested on Animals, No Added Formaldehyde, Doping Substances-free, BSE-free, Halal, Non-GMO, Zinc-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), Directive 2002/95/EC, ICH Q3D, EC No. 1935/2004, ISO 9001, Belgian Law And Codex Alimentarius Standards, Directive 1333/2008/EC, Halal, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), Regulation (EU) No. 1935/2004, United States Pharmacopeia (USP), EC No.1907/2006, Regulation (EC) No. 338/97, Directive 2011/65/EU (RoHS 2), CFDA Compliant (China), Japan DMF, EU Cosmetic Regulation 1223/2009 Compliant, ICH Q3C, Kosher, FFDCA, US DMF, National Formulary (NF), EC No. 2023/2006, EXCiPACT, Generally Recognized As Safe (GRAS), Regulation (EU) No. 10/2011 (PIM), Regulation (EU) No. 1829/2003, Directive 2001/83/EC, Directive 2009/48/EC, British Pharmacopeia (BP), Directive 2023/2055/EU, Regulation (EU) No. 1272/2008, Chinese Pharmacopeia (ChP), EU Directive 2002/72/EC, GMP, Regulation (EU) No. 1830/2003
  • Manufacturing Technology:Direct Compression
POLYOX™ WSR Coagulant LEO NF Grade is an off-white to white powder that is water soluble. It is used in dosage forms such as abuse deterrent tablets, capsules, and gels, providing essential properties for these pharmaceutical applications.

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