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IFF Pharma Solutions

37 Products found on IFF Pharma Solutions in Immediate release

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ETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty banner

IFF Pharma SolutionsETHOCEL™ Medium 70 Industrial Ethylcellulose - Specialty

Chemical Family:Cellulose Ethers, Cellulose & Cellulosics
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, 1,4-Dioxane-free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, CMR Substances-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, Indian Pharmacopeia, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, RoHS Compliant, Swiss Ordinance (SR 817.023.21), EuPIA Listed, EXCiPACT, RoHS 2 Compliant, Doping-Free, United States Pharmacopeia (USP), FDA 21 CFR 181.24, WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Japan Chemical Substances Control Law (CSCL), Majelis Ulama Indonesia Halal, Regulation (EU) No. 1169/2011, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Regulation (EU) No. 231/2012, ICH Q3C, Canadian Environmental Protection Act (CEPA), Japan Pharmacopeia (JP), Directive 2023/915/EU, ICH Q3D

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.

IFF Pharma SolutionsMETHOCEL™ A15C Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Dosage Form:Capsules, Tablets, Suspension
Labeling Claims:Low Odor, Tributyltin (TBT) - Free, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, Natural Latex Rubber-Free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Herbicide-free, PFOA-free, Antibiotics-free, Palm Oil-free, PVC-free, Diethylene Glycol-free, PAH-free, Aluminum-free, NPE-free, Pesticide-free, Paraben-free, Potassium-free, Halal, Steroids Free, Bactericide-free, CMR Substances-free, Plasticizer-free, Ethylene Glycol-free, Bisphenol A-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Perfluorocarbon (PFC)-free, Sugar-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, FSSC 22000, APE-free, Hormones-free, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Gluten-free, Fungicide-free, Low Aldehyde, Plant-Based, Radioactive-free
Certifications & Compliance:cGMP, Halal, FDA 21 CFR 172.874, Kosher, EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FDA Food Safety Modernization Act (FSMA), Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), Directive 1333/2008/EC, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, GMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ A15C Premium Methylcellulose finds applications in suspension, tablet coating, and granulation for tablets and capsules. It is used in food containers and packaging. Features include being sewage-sludge-free. Functions as a controlled release agent, immediate release agent, thickener, solubilizer, viscosity modifier, binder, film former, gelling agent, and mucoadhesive. It is water-soluble.

IFF Pharma SolutionsMETHOCEL™ K3 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Suspension
Labeling Claims:Low Odor, Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, CMR Substances-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, EU Packaging Directive (94/62/EC), British Pharmacopeia (BP), JECFA (FAO/WHO), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), WEEE Directive 2012/19/EU, European Regulation 396/2005/EC, FEMA Compliant, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU
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.

IFF Pharma SolutionsBD - 101

Chemical Name:Cellulose, Microcrystalline
Functions:Viscosity Modifier, Thickener
CAS Number:9004-34-6
Certifications & Compliance:ABNT NBR 14725, National Formulary (NF)

BD - 101 is a specialized compound comprising microcrystalline cellulose, meticulously designed to serve as an effective thickener across various pharmaceutical and nutraceutical applications, ensuring optimal performance and reliability.

IFF Pharma SolutionsAvicel® CE-15

Chemical Name:Cellulose, Microcrystalline, Calcium Hydrogen Phosphate, Guar Gum
Dosage Form:Tablets, Soft Chews
Labeling Claims:Dye Free, Natural Latex Rubber-Free, TSE-free, Perfluorooctanoic Acid-free, PFOS-free, Antibiotics-free, Sugar-free, Non-GMO, PFAS-Free, PAH-free, PVC-free, Aluminum-free, Tributyl Tin Compounds-Free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Dioxin-free, Monosodium Glutamate (MSG)-free, BSE-free, Generally Recognized As Safe (GRAS), Caffeine Free, Phthalates-free, Preservative-free, Kosher, Colorants-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegetarian, Bisphenol A-free, Latex-free, APE-free, Hormones-free
Certifications & Compliance:ICH Q3C, United States Pharmacopeia (USP), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Pharmacopeia (Ph. Eur.), FCC Compliant, cGMP, British Pharmacopeia (BP), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, FDA Food Safety Modernization Act (FSMA), EXCiPACT
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

Avicel® CE-15 a non-animal-derived ingredient, is widely employed in tablet production. It's adaptable to various manufacturing methods like direct compression, dry granulation, and wet granulation. In pharmaceutical and nutraceutical applications, it acts as a binder, compression aid, filler, immediate release agent, and suspension aid. It's supplied in powder form for easy tablet formulation.

IFF Pharma SolutionsMETHOCEL™ E6 Premium LV HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Suspension
Labeling Claims:Low Odor, Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:Halal, British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS)
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.

IFF Pharma SolutionsVitacel® VE - 650

Labeling Claims:Allergen-free, Vegetarian, Melamine-free, Vegan, BSE-free, Generally Recognized As Safe (GRAS), TSE-free, Phthalates-free, Not Listed In California Proposition 65, Nanomaterials-free
Certifications & Compliance:FDA 21 CFR Regulations, Nagoya Compliant, FDA Food Safety Modernization Act (FSMA)

Vitacel® VE - 650 boasts several labeling claims, including being BSE-free, Generally Recognized As Safe (GRAS), melamine-free, nanomaterials-free, not listed in California Proposition 65, phthalates-free, and TSE-free.

IFF Pharma SolutionsMETHOCEL™ A4C Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Labeling Claims:Low Odor, Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Nitrosamines-free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, USDA Certified, Halal, British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, National Formulary (NF), EC No.1907/2006, Japan Pharmacopeia (JP)
Manufacturing Technology: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.

IFF Pharma SolutionsMETHOCEL™ VLV Premium HPMC

Chemical Name:Hydroxypropyl Methylcellulose
CAS Number:9004-65-3
Dosage Form:Orally Disintegrating Films (ODFs), Capsules, Granules, Suspension, Tablets
Labeling Claims:APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Naturally Derived, PFAS-Free, Impurities-free, Fungicide-free, PAH-free, Plant-Based, Radioactive-free, Potassium-free, Solvent-free, Low Odor, Odor-free, Quaternary Ammonium Salt-Free, Dioxin-free, Phthalates-free, No Artificial Sweeteners, Kosher, Colorants-free, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Residues-free, Persistent Organic Pollutants (POP)-free, Herbicide-free, PFOA-free, Antibiotics-free, Palm Oil-free, Sugar-free, Low Aldehyde, PVC-free, Diethylene Glycol-free, Gluten-free, Aluminum-free, NPE-free, Pesticide-free, Steroids Free, Paraben-free, Non-Toxic, Halal, Bactericide-free, CMR Substances-free, Plasticizer-free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Perfluorocarbon (PFC)-free, Preservative-free, Glycerin-free, Artificial Flavor-Free, Vegetarian, Bisphenol A-free, FSSC 22000
Certifications & Compliance:Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, GMP, FDA 21 CFR 175.105, National Formulary (NF), European Parliament and Council Directive (E464), EC No.1907/2006, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FFDCA, FDA 21 CFR 176.180, Regulations (EU) No. 1129/2011, Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, SCF Listed, cGMP, Halal, REACH Exempt (Europe), British Pharmacopeia (BP), JECFA (FAO/WHO), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EFSA (European Food Safety Authority) Certified, EXCiPACT, CFDA Compliant (China), FDA 21 CFR 175.300, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 1935/2004, FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), Directive 2012/19/EU, Regulation (EU) No. 1169/2011, FCC Compliant, EC No. 2023/2006, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA Compliant, Directive 2011/62/EU, Directive 1333/2008/EC
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.

IFF Pharma SolutionsAccelerate® DS - 812

Chemical Name:Cellulose Gum, Croscarmellose Sodium
Dosage Form:Capsules, Granules, Tablets, Soft Chews, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Odor-free, Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 231/2012, ICH Q3C, Nagoya Compliant, FDA 21 CFR Regulations
Manufacturing Technology:Wet Granulation

Accelerate® DS - 812 contains cellulose gum and is available in capsule, granule, and orally disintegrating tablet forms. Utilizing wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical applications.

IFF Pharma SolutionsMETHOCEL™ A4M Premium Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Labeling Claims:Low Odor, Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Nitrosamines-free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, Not Listed In California Proposition 65, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP)
Manufacturing Technology:Granulation, Wet Granulation

METHOCEL™ A4M Premium Methylcellulose a water-soluble additive, is utilized in granulation and wet granulation manufacturing. It functions as a binder in ceramics and pharmaceuticals, serving as a binder, film former, and gelling agent in various applications.

IFF Pharma SolutionsMETHOCEL™ A15 Premium LV Methylcellulose

Chemical Name:Methylcellulose
CAS Number:9004-67-5
Dosage Form:Suspension
Labeling Claims:Low Odor, Odor-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, Nitrosamines-free, Hypoallergenic, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Pareve, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA 21 CFR 172.874, FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, EXCiPACT, CFDA Compliant (China), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, Regulation (EU) No. 10/2011 (PIM), European Pharmacopeia (Ph. Eur.), FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 182.1480, Regulation (EU) No. 2022/1396, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP)
Manufacturing Technology:Tablet Coating, Granulation, Wet Granulation

METHOCEL™ A15 Premium LV Methylcellulose, a versatile water-soluble excipient, is used in granulation, tablet coating, and wet granulation processes. It is employed in drug delivery solutions for oral healthcare and in industrial applications for ceramics and refractory materials. It functions as a binder, disintegrant, emulsifier, and stabilizer.

IFF Pharma SolutionsLattice® NT 200 - Specialty

Functions:Binder
Chemical Family:Cellulose & Cellulosics

Lattice® NT 200 - Specialty is tailored for tablet manufacturing, facilitating direct compression and wet granulation processes. As a binder and disintegrant, it ensures tablet integrity and rapid dissolution. Identified as cellulose and cellulosics, particularly microcrystalline cellulose, it offers water-dispersible granules (WDG) for enhanced formulation efficiency.

IFF Pharma SolutionsAc-Di-Sol® SD - 711

Chemical Name:Croscarmellose Sodium
CAS Number:74811-65-7
Dosage Form:Capsules, Granules, Orally Disintegrating Tablets (ODTs)
Labeling Claims:Melamine-free, Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Nanomaterials-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, TSE-free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, Triphenyl Tin Compounds-Free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, Not Listed In California Proposition 65, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:Halal, British Pharmacopeia (BP), China DMF, FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, GMP, Nagoya Compliant, National Formulary (NF), FDA 21 CFR Regulations, Japan Pharmacopeia (JP)
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.

IFF Pharma SolutionsAquateric® N100

Dosage Form:Tablets, Capsules
Labeling Claims:Kosher, Non-GMO
Certifications & Compliance:Kosher

Aquateric® N100 available in powder form, is suitable for various dosage forms, such as capsules and tablets, particularly in dietary supplements. It serves as a release agent in food applications and offers the benefit of being non-GMO. Utilized in tablet coating manufacturing technology, it functions as an enteric coating system and an extended-release agent in pharmaceutical and nutraceutical products.

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