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IFF Pharma Solutions

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169 Products found on IFF Pharma Solutions  in Pharmaceuticals & Nutraceuticals

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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.
Avicel® CL - 611 banner
IFF Pharma SolutionsAvicel® CL - 611
  • Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
  • Dosage Form:Spray, Suspension
  • Labeling Claims:Triphenyl Tin Compounds-Free, Genotoxic-free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free, Allergen-free, Monosodium Glutamate (MSG)-free, PFOS-free, Nitrosamines-free, Hormones-free, Free of Major Allergens, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Melamine-free, Colorants-free, Amine-free, Latex-free, Dioxin-free, Animal Products-free, Flavor Free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Not Tested on Animals, Tributyl Tin Compounds-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Irradiation-free, Gluten-free, BSE-free, Sugar-free, PVC-free, Dye Free, Dehp (Diethylhexyl Phthalate)-Free, Mycotoxins-free, Perfluorooctanoic Acid-free, Glycerin-free
  • Certifications & Compliance:FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), ICH Q3C, European Pharmacopeia (Ph. Eur.), JECFA (FAO/WHO), Kosher, Regulation (EC) No. 1334/2008, Regulation (EU) No. 1829/2003, GMP, Halal, Halal, Central Islamic Council of Thailand, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Japanese Pharmaceutical Excipients (JPE), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, ISO 45001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, British Pharmacopeia (BP), Union of Orthodox Jewish Congregations of America Kosher
  • Manufacturing Technology:Wet Granulation, Dry Granulation, Direct Compression
Avicel® CL - 611 a non-animal-origin ingredient, is used in sprays and suspensions. It's compatible with various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceuticals, it acts as a binder, filler, stabilizer, and immediate release agent. It's also an emulsifying agent and viscosity modifier, aiding suspension.
Viscarin® PH - 209NF banner
IFF Pharma SolutionsViscarin® PH - 209NF
  • Chemical Name:Carrageenan
  • CAS Number:9000-07-1
  • Dosage Form:Soft Gels
  • Labeling Claims:Monosodium Glutamate (MSG)-free, PFOS-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Colorants-free, Dioxin-free, Animal Products-free, GMO-free, Natural Latex Rubber-Free, COSMOS Approved, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Organic, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Halal, Paraben-free, Aluminum-free, Preservative-free
  • Certifications & Compliance:EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA 21 CFR 177.1520, European Commission Decision 97/534/EC, European Pharmacopeia (Ph. Eur.), FDA 21 CFR 179.26, Regulation (EU) No. 1829/2003, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, IFANCA Halal, ISO 9001, Regulation (EU) No. 1830/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), FDA 7 CFR 205.605, Orthodox Union Kosher, ABNT NBR 14725, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), cGMP, Regulation (EU) No. 1169/2011, Regulation (EU) No. 1272/2008, IFRA Compliant
  • Manufacturing Technology:Encapsulation
Viscarin® PH - 209NF utilizes encapsulation technology and is GMO-free, non-GMO, BSE-free, TSE-free, and palm oil-free. It caters to healthcare and pharma markets, particularly in oral drug delivery and care solutions. It serves as both an emulsifier and stabilizer and aids in formulation and processing in pharmaceutical and nutraceutical applications, including modified and controlled release formulations.
SeaGel® CAP - 202 banner
IFF Pharma SolutionsSeaGel® CAP - 202
  • Chemical Name:Hydroxypropyl Starch, Carrageenan
  • Functions:Encapsulant
  • Labeling Claims:Hormones-free, Phthalates-free, Colorants-free, Paraben-free, Natural Latex Rubber-Free, Naturally Derived, Vegan, Halal, Triphenyl Tin Compounds-Free, Kosher, Non-GMO, PHO (Partially Hydrogenated Oil)-Free, Sustainable, Environmentally Friendly, Plasticizer-free, PAH-free, Pesticide-free, GMO-free, Palm Oil-free, Sugar-free, APE-free, Dye Free, PFAS-Free, Generally Recognized As Safe (GRAS), Vegetarian, Aluminum-free, Natural, Endocrine Disruptor-free, PVC-free, TSE-free, PFOS-free, Pareve, Perfluorooctanoic Acid-free, Preservative-free, Tributyl Tin Compounds-Free, Nitrosamines-free, BSE-free, Glycerin-free, Bisphenol A-free, Dioxin-free, Caffeine Free, Antibiotics-free, Animal Products-free, Monosodium Glutamate (MSG)-free
  • Certifications & Compliance:cGMP, Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, European Regulation 396/2005/EC, FSSC 22000, ISO 9001, Halal, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Doping-Free, IFANCA Halal, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, Regulation (EU) No. 1169/2011, Orthodox Union Kosher, EC No.1907/2006, Directive 396/2005/EC, FDA 21 CFR 177.1520, FDA 21 CFR 179.26, IFRA Compliant, Regulation (EU) No. 1272/2008
  • Dosage Form:Capsules
SeaGel® CAP - 202 ideal for capsules, utilizes encapsulation technology. It meets labeling claims like non-GMO, BSE-free, TSE-free, palm oil-free, glycerin-free, and endocrine disruptor-free, ensuring suitability for vegetarians. Its applications span food, nutrition, healthcare, and pharmaceuticals, serving in nutraceuticals, supplements, and oral drug delivery.
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.
METHOCEL™ VLV Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ VLV Premium HPMC
  • INCI Name:Methylcellulose
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Dosage Form:Granules, Tablets, Capsules, Suspension, Orally Disintegrating Films (ODFs)
  • Labeling Claims:Vegan, Low Odor, Phthalates-free, Steroids Free, Zero Calorie, Paraben-free, Nitrosamines-free, Aluminum-free, Preservative-free, Allergen-free, Halal, Radioactive-free, Potassium-free, PAH-free, Caffeine Free, Sewage Sludge Free, Colorants-free, Artificial Flavor-Free, Herbicide-free, NPE-free, PFOA-free, Diethylene Glycol-free, Gluten-free, PHO (Partially Hydrogenated Oil)-Free, Persistent Organic Pollutants (POP)-free, Monosodium Glutamate (MSG)-free, VOC-free, Non-Toxic, Pareve, Endocrine Disruptor-free, Plant-Based, Quaternary Ammonium Salt-Free, Dioxin-free, Vegetarian, Non-GMO, Palm Oil-free, Ethylene Glycol-free, USP 232 Elemental Impurities Free, Solvent-free, Kosher, Bisphenol A-free, PFAS-Free, Antibiotics-free, Hormones-free, PVC-free, Naturally Derived, Organic, Tributyltin (TBT) - Free, Residues-free, Bactericide-free, No Artificial Sweeteners, APE-free, Odor-free, Pesticide-free, Low Aldehyde, CMR Substances-free, Plasticizer-free, Irradiation-free, Glycerin-free, Sugar-free, PFOS-free, Fungicide-free, Perfluorocarbon (PFC)-free, Natural Latex Rubber-Free, FSSC 22000, Impurities-free
METHOCEL™ VLV Premium HPMC is a versatile industrial additive designed for various applications, including tablet coating, orally disintegrating films, capsules, suspensions, and granules. With high efficiency and water solubility, it offers excellent cohesion development, green strength, and water retention. It functions as a binder, emulsifier, lubricant, and surfactant make it indispensable across manufacturing processes. Additionally, it serves as a water retention agent, binder and resin, slip agent, coating system, mucoadhesive, film former, viscosity modifier, solubilizer, gelling agent, and immediate release agent. METHOCEL™ VLV Premium HPMC's improved pumpability and lubricating properties ensure easy handling, making it a go-to choice for industrial and pharmaceutical formulations.
Manucol® LD banner
IFF Pharma SolutionsManucol® LD
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Not Listed In California Proposition 65, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Palm Oil-free, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free, Halal, Paraben-free, Aluminum-free
  • Certifications & Compliance:IFRA Compliant, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, Belgian Law And Codex Alimentarius Standards, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Chinese Pharmacopeia (ChP), British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Regulation (EU) No. 1272/2008
  • Chemical Inventories:PICCS (Phillipines), AICS (Australia), NDSL (Canada), ENCS (Japan), ECL (Korea), DSL (Canada), IECSC (China), TSCA (USA)
Manucol® LD composed of sodium alginate, serves various pharmaceutical and nutraceutical functions, including antacid properties, controlled release, gelling, stabilization, and thickening.
SeaGel® CAP - 101 banner
IFF Pharma SolutionsSeaGel® CAP - 101
  • Chemical Name:Carrageenan
  • Functions:Encapsulant
  • Labeling Claims:Hormones-free, Phthalates-free, Colorants-free, Paraben-free, Natural Latex Rubber-Free, Naturally Derived, Vegan, Halal, Triphenyl Tin Compounds-Free, Kosher, Non-GMO, PHO (Partially Hydrogenated Oil)-Free, Sustainable, Environmentally Friendly, Plasticizer-free, PAH-free, Pesticide-free, GMO-free, Palm Oil-free, Sugar-free, APE-free, Dye Free, PFAS-Free, Generally Recognized As Safe (GRAS), Vegetarian, Aluminum-free, Natural, Endocrine Disruptor-free, PVC-free, TSE-free, PFOS-free, Pareve, Perfluorooctanoic Acid-free, Preservative-free, Tributyl Tin Compounds-Free, Nitrosamines-free, BSE-free, Glycerin-free, Bisphenol A-free, Dioxin-free, Caffeine Free, Antibiotics-free, Animal Products-free, Monosodium Glutamate (MSG)-free
  • Certifications & Compliance:cGMP, Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 7 CFR 205.605, European Regulation 396/2005/EC, FSSC 22000, ISO 9001, Halal, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Generally Recognized As Safe (GRAS), Regulation (EU) No. 1830/2003, Doping-Free, IFANCA Halal, Hazard Analysis Critical Control Point (HACCP), European Commission Decision 97/534/EC, Regulation (EU) No. 1169/2011, Orthodox Union Kosher, EC No.1907/2006, Directive 396/2005/EC, FDA 21 CFR 177.1520, FDA 21 CFR 179.26, IFRA Compliant, Regulation (EU) No. 1272/2008
  • Dosage Form:Capsules
SeaGel® CAP - 101 ideal for capsules, utilizes encapsulation technology. It meets labeling claims like non-GMO, BSE-free, TSE-free, palm oil-free, glycerin-free, and endocrine disruptor-free, ensuring suitability for vegetarians. Its applications span food, nutrition, healthcare, and pharmaceuticals, serving in nutraceuticals, supplements, and oral drug delivery.
Protanal® CR - 8133 banner
IFF Pharma SolutionsProtanal® CR - 8133
  • Chemical Name:Sodium Alginate
  • Labeling Claims:Halal, Paraben-free, Aluminum-free, Preservative-free, Monosodium Glutamate (MSG)-free, Copper-free, PFOS-free, Residual Solvent -Free, Nitrosamines-free, Hormones-free, PHO (Partially Hydrogenated Oil)-Free, Caffeine Free, Kosher, Pesticide-free, Solvent-free, Antibiotics-free, Barium-free, Cadmium-free, Colorants-free, Dioxin-free, Cobalt-free, GMO-free, Natural Latex Rubber-Free, Phthalates-free, PFAS-Free, Non-GMO, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Odor-free, TSE-free, Palm Oil-free, Vegetarian, Pareve, Ethylene Oxide-free, Bisphenol A-free, Generally Recognized As Safe (GRAS), APE-free, BSE-free, Sugar-free, PVC-free, Dye Free, Endocrine Disruptor-free, Perfluorooctanoic Acid-free, Glycerin-free, Triphenyl Tin Compounds-Free, Gold-Free, Plasticizer-free
  • Certifications & Compliance:Regulation (EU) No. 1272/2008, IFRA Compliant, Halal Food Council of Europe, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), Japan Pharmacopeia (JP), European Pharmacopeia (Ph. Eur.), ISO 9000, Kosher, GMP, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, EXCiPACT, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, EU Cosmetic Regulation 1223/2009 Compliant, FCC Compliant, British Pharmacopeia (BP), FSSC 22000, Hazard Analysis Critical Control Point (HACCP)
Protanal® CR - 8133 featuring sodium alginate, serves various functions in pharmaceuticals and nutraceuticals. It acts as controlled release agent, emulsifying agent, gelling agent, thickener, and viscosity modifier, available in powder form.
ETHOCEL™ Standard 14 Premium Ethylcellulose banner
IFF Pharma SolutionsETHOCEL™ Standard 14 Premium Ethylcellulose
  • Chemical Name:Ethylcellulose
  • CAS Number:9004-57-3
  • Functions:Controlled Release Agent, Granulation Aid, Binder, Taste Masker
  • 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, EC No. 1935/2004, 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, EC No. 2023/2006, 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), EU Directive 2002/72/EC, GMP
  • Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Encapsulation, Direct Compression
ETHOCEL™ Standard 14 Premium Ethylcellulose available in powder form, is adaptable for various manufacturing processes such as direct compression, encapsulation, and granulation. It exhibits ethanol solubility, offering versatility in pharmaceutical and industrial applications.

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