Immediate release

36 Products found in Immediate release

ETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty banner
IFF Pharma SolutionsETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty
  • Chemical Name:Ethylcellulose
  • Chemical Family:Cellulose & Cellulosics, Cellulose Ethers
  • CAS Number:9004-57-3
  • Dosage Form:Tablets
  • Labeling Claims:Dioxin-free, Paraben-free, Aflatoxin-free, Triphenyl Tin Compounds-Free, Halal, PFOS-free, Phthalates-free, Nitrosamines-free, Sugar-free, Irradiation-free, PHO (Partially Hydrogenated Oil)-Free, Palm Oil-free, APE-free, Allergen-free, Antibiotics-free, Colorants-free, TSE-free, Formaldehyde-free, Plasticizer-free, Dairy-free, BSE-free, Glycerin-free, Dye Free, Endocrine Disruptor-free, VOC-free, Hormones-free, Bisphenol A-free, PAH-free, Preservative-free, 1,4-Dioxane-free, Mycotoxins-free, Aluminum-free, Caffeine Free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, Sewage Sludge Free, Organic, Monosodium Glutamate (MSG)-free, Kosher, PFAS-Free, CMR Substances-free, Tributyl Tin Compounds-Free, Zero Calorie, PVC-free, Pesticide-free
  • Certifications & Compliance:Clean Air Act (CAA) Certified, Indian Pharmacopeia, EU Cosmetic Regulation 1223/2009 Compliant, European Regulation 396/2005/EC, FDA 21 CFR 163, Regulation (EU) No. 10/2011 (PIM), ISO 9001, RoHS 2 Compliant, United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, Regulation (EU) No. 1169/2011, GMP, FCC Compliant, Japan Chemical Substances Control Law (CSCL), Japan Pharmacopeia (JP), USDA Organic, Turkish RoHS Regulation, Canadian Environmental Protection Act (CEPA), Regulation (EC) No. 1333/2008, Doping-Free, Directive 2009/48/EC, Majelis Ulama Indonesia Halal, Chinese Pharmacopeia (ChP), FDA Compliant, FDA 21 CFR 181.24, cGMP, FSSC 22000, Swiss Ordinance (SR 817.023.21), ICH Q3C, EuPIA Listed, WEEE Directive 2012/19/EU, Organic Certified, FDA Food Safety Modernization Act (FSMA), Directive 2023/915/EU, Regulation (EU) No. 231/2012, RoHS Compliant, Kosher, FDA 21 CFR 101.9
  • Manufacturing Technology:Encapsulation, Direct Compression, Granulation, Tablet Coating
ETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty offers binding and controlled release properties along with excellent flexibility and thermal stability. It's compatible with varnishes, lacquers, and hot melt coating processes, and is soluble in ethanol.
METHOCEL™ E6 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ E6 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Lubricant (Internal), Surfactant, Emulsifier, Binder, Mucoadhesive, Immediate Release Agent, Film Former, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Suspension, Tablets
  • Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FFDCA, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ E6 Premium LV HPMC is water-soluble and used in suspensions, granulation, and tablet coating. It serves as a binder, controlled release agent, immediate release agent, mucoadhesive, and solubilizer in pharmaceuticals and nutraceuticals, and as a binder in ceramics.
METHOCEL™ K3 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ K3 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Controlled Release Agent, Binder, Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Suspension, Tablets
  • Labeling Claims:VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, CMR Substances-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), JECFA (FAO/WHO), Kosher, FEMA Compliant, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, WEEE Directive 2012/19/EU, FDA Compliant, Doping-Free, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Swiss Ordinance (SR 817.023.21), EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ K3 Premium LV HPMC utilized in ceramics and pharmaceuticals, serves as a binder, controlled release agent, film former, gelling agent, immediate release agent, and mucoadhesive, facilitating suspension and tablet coating. Its water solubility adds versatility in various applications.
METHOCEL™ A4C Premium Methylcellulose banner
IFF Pharma SolutionsMETHOCEL™ A4C Premium Methylcellulose
  • Chemical Name:Methylcellulose
  • CAS Number:9004-67-5
  • Functions:Rheology Modifier, Plasticizer, Controlled Release Agent, Lubricant (Internal), Suspending Agent, Surfactant, Emulsifier, Binder, Thickener, Mucoadhesive, Film Former, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Tablets
  • Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, Melamine-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Halal, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), FFDCA, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FSSC 22000, FDA Food Safety Modernization Act (FSMA), USDA Certified, Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Directive 1333/2008/EC, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ A4C Premium Methylcellulose manufactured using granulation technology, serves various functions in pharmaceutical and nutraceutical applications. It acts as a binder, film former, gelling agent, mucoadhesive, thickener, and viscosity modifier, ensuring optimal performance and formulation versatility.
Protanal® Ester K3B426 banner
IFF Pharma SolutionsProtanal® Ester K3B426
  • Chemical Name:Propyleneglycol alginate
  • CAS Number:9005-37-2
  • Labeling Claims:Colorants-free, Copper-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Propylene Glycol-free, Pareve, Solvent-free, Mycotoxins-free, Residual Solvent -Free, APE-free, Caffeine Free, Dye Free, Barium-free, Melamine-free, Mercury-Free, Monosodium Glutamate (MSG)-free, PAH-free, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Cobalt-free, Gold-Free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, TSE-free, Vegetarian, Cadmium-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Animal Products-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), ISO 9000, JECFA (FAO/WHO), GMP, Kosher, Doping-Free, ISO 14001, National Formulary (NF), Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 10/2011 (PIM), Generally Recognized As Safe (GRAS), FCC Compliant, British Pharmacopeia (BP), EU Packaging Directive (94/62/EC), FSSC 22000, Hazard Analysis Critical Control Point (HACCP), EC No. 2023/2006, Regulation (EU) No. 1830/2003, Regulation (EU) No. 1935/2004, IFRA Compliant
Protanal® Ester K3B426 ensures peace of mind with its labeling claims of being free from bisphenol A, caffeine, colorants, and dioxin. This versatile powder serves multiple functions in pharmaceuticals, belonging to both excipients and active pharmaceutical ingredients (APIs) categories.
Endurance® VE - 101 banner
IFF Pharma SolutionsEndurance® VE - 101
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Functions:Binder
  • Manufacturing Technology:Direct Compression, Wet Granulation
  • Labeling Claims:Dye Free, Plasticizer-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Not Tested on Animals, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, PFAS-Free, Zinc-free, Aluminum-free, Endocrine Disruptor-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Kosher, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), ISO 45001, ISO 14001, Orthodox Union Kosher, National Formulary (NF), FCC Compliant, ISO 22000, Generally Recognized As Safe (GRAS)
Endurance® VE - 101 containing microcrystalline cellulose, is utilized in dietary supplements for its binding properties. It serves as a binder in both food and pharmaceutical applications, providing structural integrity in powder form.
METHOCEL™ VLV Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ VLV Premium HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Mucoadhesive, Immediate Release Agent, Viscosity Modifier, Gelling Agent, Controlled Release Agent, Coating System, Binder, Thickener, Solubilizer, Film Former
  • Dosage Form:Capsules, Tablets, Suspension, Orally Disintegrating Films (ODFs), Granules
  • Labeling Claims:Sewage Sludge Free, Odor-free, Quaternary Ammonium Salt-Free, Halal, Tributyltin (TBT) - Free, USP 232 Elemental Impurities Free, Paraben-free, Gluten-free, PAH-free, PFOS-free, Zero Calorie, Caffeine Free, Perfluorocarbon (PFC)-free, Bisphenol A-free, Glycerin-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Herbicide-free, Palm Oil-free, Solvent-free, Pesticide-free, No Artificial Sweeteners, Low Aldehyde, Diethylene Glycol-free, Irradiation-free, Nitrosamines-free, PFAS-Free, Impurities-free, Aluminum-free, Endocrine Disruptor-free, PFOA-free, NPE-free, CMR Substances-free, Naturally Derived, Plasticizer-free, APE-free, Vegetarian, FSSC 22000, Steroids Free, Non-GMO, Monosodium Glutamate (MSG)-free, Phthalates-free, Residues-free, Allergen-free, Vegan, Antibiotics-free, Radioactive-free, Kosher, Ethylene Glycol-free, Fungicide-free, Hormones-free, Low Odor, Preservative-free, Natural Latex Rubber-Free, Bactericide-free, Organic, Colorants-free, Plant-Based, PVC-free, Non-Toxic, VOC-free, Persistent Organic Pollutants (POP)-free, Potassium-free
  • Certifications & Compliance:Japan Pharmacopeia (JP), FDA 21 CFR 174.5, JECFA (FAO/WHO), EC No. 2023/2006, SCF Listed, FSSC 22000, Regulation (EU) No. 231/2012, ISO 9001, Directive 1333/2008/EC, Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Indian Pharmacopeia, Regulation (EU) No. 1272/2008, EU Cosmetic Regulation 1223/2009 Compliant, European Parliament and Council Directive (E464), FDA 21 CFR 176.170, Regulation (EU) No. 1935/2004, National Formulary (NF), FDA 21 CFR 175.300, Directive 2009/48/EC, Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, FFDCA, Kosher, European Regulation 396/2005/EC, ICH Q3C, EC No.1907/2006, FDA Food Safety Modernization Act (FSMA), FDA Compliant, Belgian Law And Codex Alimentarius Standards, Doping-Free, FDA 21 CFR 176.180, EC No. 1935/2004, Halal, Directive 2023/915/EU, FDA 21 CFR 172.874, FDA 21 CFR 175.105, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), Orthodox Union Kosher, Regulation (EC) No. 1333/2008, CFDA Compliant (China), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, Regulations (EU) No. 1129/2011, USDA Organic, EXCiPACT, Directive 2011/62/EU, EFSA (European Food Safety Authority) Certified, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP), REACH Exempt (Europe), EU Directive 2002/72/EC, cGMP
  • Manufacturing Technology:Tablet Coating, Wet Granulation
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.
METHOCEL™ E3 Premium LV HPMC banner
IFF Pharma SolutionsMETHOCEL™ E3 Premium LV HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Functions:Sustained Release Agent, Rheology Modifier, Plasticizer, Controlled Release Agent, Lubricant (Internal), Surfactant, Emulsifier, Binder, Thickener, Mucoadhesive, Immediate Release Agent, Film Former, Viscosity Modifier, Gelling Agent, Solubilizer, Film Former
  • Dosage Form:Suspension, Tablets
  • Labeling Claims:PVC-free, Perfluorooctanoic Acid-free, VOC-free, Nitrosamines-free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Dye Free, Naturally Derived, Plasticizer-free, Sewage Sludge Free, APE-free, Odor-free, Triphenyl Tin Compounds-Free, Vegetarian, Residual Solvent -Free, Halal, USP 232 Elemental Impurities Free, Paraben-free, PAH-free, PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Zero Calorie, Caffeine Free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, Vegan, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Hypoallergenic, Antibiotics-free, Aflatoxin-free, TSE-free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Low Odor, BSE-free, Palm Oil-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Organic, Colorants-free, Plant-Based, Irradiation-free
  • Certifications & Compliance:Regulation (EU) No. 1830/2003, Directive 2009/48/EC, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), GMP, Generally Recognized As Safe (GRAS), FDA 21 CFR 101.9, cGMP, Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), FFDCA, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, Halal, FDA 21 CFR 172.874, European Pharmacopeia (Ph. Eur.), EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), Organic Certified, ISO 14001, Regulation (EU) No. 1829/2003, FDA 21 CFR 182.1480, Orthodox Union Kosher, Indian Pharmacopeia, Regulation (EC) No. 1333/2008, Regulation (EU) No. 1272/2008, CFDA Compliant (China), Regulation (EU) No. 1169/2011, National Formulary (NF), FCC Compliant, Regulation (EU) No. 2022/1396, USDA Organic, EXCiPACT
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ E3 Premium LV HPMC suitable for suspensions, offers binding properties crucial for ceramic applications. With granulation and tablet coating manufacturing technologies, it ensures efficient production processes. Additionally, its water solubility makes it ideal for pharmaceutical and nutraceutical applications, serving as a binder and controlled release agent.
Protanal® PH - 8133 banner
IFF Pharma SolutionsProtanal® PH - 8133
  • Chemical Name:Sodium Alginate
  • Ingredient Name:Sodium Alginate
  • CAS Number:9005-38-3
  • Labeling Claims:Gold-Free, PFAS-Free, Aluminum-free, Endocrine Disruptor-free, Dye Free, Plasticizer-free, Nanomaterials-free, Copper-free, Barium-free, APE-free, Triphenyl Tin Compounds-Free, Vegetarian, Residual Solvent -Free, Halal, Paraben-free, Cadmium-free, Propylene Glycol-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Mycotoxins-free, Pareve, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, BSE-free, Palm Oil-free, Solvent-free, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, Cobalt-free, PVC-free, Perfluorooctanoic Acid-free, Nitrosamines-free, Melamine-free
  • Certifications & Compliance:GMP, Generally Recognized As Safe (GRAS), Japan Pharmacopeia (JP), Hazard Analysis Critical Control Point (HACCP), JECFA (FAO/WHO), EC No. 2023/2006, Kosher, European Regulation 396/2005/EC, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, FDA Compliant, Doping-Free, European Pharmacopeia (Ph. Eur.), IFRA Compliant, EU Packaging Directive (94/62/EC), United States Pharmacopeia (USP), Regulation (EU) No. 10/2011 (PIM), ISO 14001, Regulation (EU) No. 1829/2003, Regulation (EU) No. 1272/2008, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1935/2004, National Formulary (NF), FCC Compliant, ISO 9000, EXCiPACT, Regulation (EU) No. 1830/2003, British Pharmacopeia (BP)
  • Chemical Inventories:NDSL (Canada), ECL (Korea), PICCS (Phillipines), ENCS (Japan), IECSC (China), DSL (Canada), AICS (Australia)
Protanal® PH - 8133 is a trusted choice, ensuring compliance with various labeling claims, including being non-GMO, solvent-free, and devoid of residual solvents, BSE, TSE, palm oil, mercury, copper, and cobalt. Its versatility extends to pharmaceutical applications, serving as emulsifiers, stabilizers, and aids in modified and controlled release formulations.
Ac-Di-Sol® SD - 711 banner
IFF Pharma SolutionsAc-Di-Sol® SD - 711
  • Chemical Name:Croscarmellose Sodium
  • CAS Number:74811-65-7
  • Dosage Form:Orally Disintegrating Tablets (ODTs), Granules, Capsules
  • Labeling Claims:Not Tested on Animals, Not Listed In California Proposition 65, Colorants-free, Ethylene Oxide-free, Natural Latex Rubber-Free, Halal, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, APE-free, Caffeine Free, Dye Free, Melamine-free, Monosodium Glutamate (MSG)-free, Artificial Flavor-Free, PAH-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, USP 232 Elemental Impurities Free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, Endocrine Disruptor-free, Vegetarian, TSE-free, Palm Oil-free, Phthalates-free, Pesticide-free, Aflatoxin-free, Tributyl Tin Compounds-Free, GMO-free, Kosher, Preservative-free, PFAS-Free, Nanomaterials-free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), GMP, Kosher, Halal, Doping-Free, ISO 14001, National Formulary (NF), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), FDA 21 CFR Regulations, FCC Compliant, British Pharmacopeia (BP), Nagoya Compliant, ISO 45001, FSSC 22000, Orthodox Union Kosher, Regulation (EU) No. 1169/2011, IFANCA Halal, China DMF
  • Manufacturing Technology:Wet Granulation
Ac-Di-Sol® SD - 711 a powdered form of croscarmellose sodium, is utilized as a disintegrant and immediate release agent in pharmaceuticals and nutraceuticals. Its versatility is evident in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs), manufactured through wet granulation techniques.
Endurance® VE - 102 banner
IFF Pharma SolutionsEndurance® VE - 102
  • Chemical Name:Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Functions:Binder
  • Manufacturing Technology:Direct Compression, Wet Granulation
  • Labeling Claims:Dye Free, Plasticizer-free, APE-free, Triphenyl Tin Compounds-Free, Halal, Paraben-free, PAH-free, Generally Recognized As Safe (GRAS), PFOS-free, Non-GMO, Ethylene Oxide-free, Monosodium Glutamate (MSG)-free, Caffeine Free, GMO-free, Bisphenol A-free, Glycerin-free, Phthalates-free, Allergen-free, Artificial Flavor-Free, PHO (Partially Hydrogenated Oil)-Free, Dioxin-free, Not Listed In California Proposition 65, Sugar-free, Antibiotics-free, Latex-free, Aflatoxin-free, TSE-free, Mercury-Free, Kosher, Animal Products-free, Tributyl Tin Compounds-Free, Hormones-free, Palm Oil-free, BSE-free, Solvent-free, Not Tested on Animals, Preservative-free, Pesticide-free, Natural Latex Rubber-Free, Colorants-free, Irradiation-free, PVC-free, Perfluorooctanoic Acid-free, PFAS-Free, Zinc-free, Aluminum-free, Endocrine Disruptor-free
  • Certifications & Compliance:cGMP, Japan Pharmacopeia (JP), Kosher, European Regulation 396/2005/EC, ICH Q3C, FSSC 22000, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 231/2012, ISO 9001, Doping-Free, Halal, European Pharmacopeia (Ph. Eur.), United States Pharmacopeia (USP), ISO 45001, ISO 14001, Orthodox Union Kosher, National Formulary (NF), FCC Compliant, ISO 22000, Generally Recognized As Safe (GRAS)
Endurance® VE - 102 comprising microcrystalline cellulose, finds applications in dietary supplements. It functions as a binder in food and nutrition, as well as in pharmaceuticals and nutraceuticals, presenting as a powder.
Avicel® CL - 611 banner
IFF Pharma SolutionsAvicel® CL - 611
  • Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
  • Dosage Form:Suspension, Spray
  • Labeling Claims:Not Tested on Animals, Ethylene Oxide-free, Colorants-free, Natural Latex Rubber-Free, Halal, Nitrosamines-free, BSE-free, Perfluorooctanoic Acid-free, PVC-free, Hormones-free, Glycerin-free, Plasticizer-free, Gluten-free, Solvent-free, Mycotoxins-free, APE-free, Caffeine Free, Dye Free, Genotoxic-free, Flavor Free, Melamine-free, Monosodium Glutamate (MSG)-free, PAH-free, Odor-free, Free of Major Allergens, Latex-free, PFOS-free, Antibiotics-free, Allergen-free, Irradiation-free, Non-GMO, Generally Recognized As Safe (GRAS), Paraben-free, Dioxin-free, Sugar-free, Aluminum-free, Bisphenol A-free, Triphenyl Tin Compounds-Free, PHO (Partially Hydrogenated Oil)-Free, TSE-free, Vegetarian, Palm Oil-free, Phthalates-free, Pesticide-free, Animal Products-free, Tributyl Tin Compounds-Free, Kosher, Amine-free, Dehp (Diethylhexyl Phthalate)-Free, Preservative-free, PFAS-Free, Vegan
  • Certifications & Compliance:Japan Pharmacopeia (JP), EXCiPACT, European Pharmacopeia (Ph. Eur.), Japanese Pharmaceutical Excipients (JPE), JECFA (FAO/WHO), GMP, Kosher, Halal, ISO 14001, National Formulary (NF), Directive 1169/2011/EC, Halal Food Council of Europe, European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, ISO 9001, United States Pharmacopeia (USP), FDA Compliant, Regulation (EU) No. 1829/2003, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EU) No. 1272/2008, Regulation (EC) No. 1334/2008, FDA Food Safety Modernization Act (FSMA), Chinese Pharmacopeia (ChP), ISO 22000, Regulation (EU) No. 1881/2006, Halal, Central Islamic Council of Thailand, Generally Recognized As Safe (GRAS), British Pharmacopeia (BP), ISO 45001, cGMP, FSSC 22000, Hazard Analysis Critical Control Point (HACCP), Union of Orthodox Jewish Congregations of America Kosher, Regulation (EU) No. 1830/2003, IFANCA Halal, IFRA Compliant
  • Manufacturing Technology:Dry Granulation, Direct Compression, Wet Granulation
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.

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