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130 Products found on IFF Pharma Solutions in Drug Delivery & Care Solutions

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IFF Pharma SolutionsMETHOCEL™ K200M Premium CR 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, National Bioengineered Food Disclosure Standard, 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, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU
Manufacturing Technology:Tablet Coating, Granulation

METHOCEL™ K200M Premium CR HPMC used in ceramics and pharmaceuticals, acts as a binder and enables immediate release in suspensions and tablet coatings. It also serves as a film former, gelling agent, mucoadhesive, and solubilizer, offering versatile applications due to its water solubility.

IFF Pharma SolutionsPRONOVA® UP LVM

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® UP LVM is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.

IFF Pharma SolutionsPOLYOX™ WSR - 303 FP NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Dosage Form:Gels, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules, Tablets
Labeling Claims:Plant-Based, Residual Solvent -Free, Halal, Chlorine-free, Ethylene Glycol-free, Not Tested on Animals, Kosher, Allergen-free, No Added Formaldehyde, Vegetarian, Vegan, Nitrosamines-free, Naturally Derived, Heavy Metal-free, Not Listed In California Proposition 65, Diethylene Glycol-free
Certifications & Compliance:Japan Pharmacopeia (JP), US DMF, European Pharmacopeia (Ph. Eur.), Belgian Law And Codex Alimentarius Standards, ICH Q3D, Halal, Japan DMF, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), Kosher, Clean Water Act (CWA) Certified, EXCiPACT, CFDA Compliant (China), ICH Q3C, GMP, United States Pharmacopeia (USP), National Formulary (NF)
Manufacturing Technology:Direct Compression

POLYOX™ WSR - 303 FP NF Grade with its off-white powdered form, serves various functions in cleaning ingredients, acting as a binder and thickener. It finds application in diverse dosage forms such as gels, osmotic pump tablets, and conventional tablets, leveraging its water solubility and facilitating controlled release in pharmaceutical and nutraceutical formulations, manufactured through direct compression technology.

IFF Pharma SolutionsPRONOVA® UP LVG

Chemical Name:Sodium Alginate
Dosage Form:Foams
Labeling Claims:Biodegradable, High Purity, Biocompatible
Certifications & Compliance:EC No.1907/2006, Directive 2023/2055/EU
Manufacturing Technology:Encapsulation

PRONOVA® UP LVG is available in foam form with labeling claims of high purity and biodegradability. It contains sodium alginate, serves as an emulsifier and stabilizer, and is a is a modified and controlled release excipient. The product is supplied in solution form.

IFF Pharma SolutionsAvicel® RC - 591

Chemical Name:Cellulose, carboxymethyl ether, sodium salt, Cellulose, Microcrystalline
Dosage Form:Lotions, Suspension, Spray
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, 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, Latex-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Japanese Pharmaceutical Excipients (JPE), Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, GMP, National Formulary (NF), Generally Recognized As Safe (GRAS)
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

Avicel® RC - 591 is versatile, catering to various dosage forms like lotions, sprays, and suspensions. Its manufacturing technology involves direct compression, dry granulation, and wet granulation methods. In pharmaceutical and nutraceutical applications, it serves as a binder, compression aid, immediate release agent, and stabilizer, ensuring product efficacy and stability.

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 SolutionsETHOCEL™ Standard 14 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, 1,4-Dioxane-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, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, Halal, British Pharmacopeia (BP), 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, FDA 21 CFR 172.868, CFDA Compliant (China), 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, FCC Compliant, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 573.420, ICH Q3C, Canadian Environmental Protection Act (CEPA), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Direct Compression, Encapsulation

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.

IFF Pharma SolutionsMETHOCEL™ E5 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, Not Listed In California Proposition 65, 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™ E5 Premium LV HPMC is water-soluble and used in suspensions, granulation, and tablet coating. It functions as a binder, controlled release agent, film former, and gelling agent in pharmaceuticals and nutraceuticals, and as a binder in ceramics.

IFF Pharma SolutionsETHOCEL™ Standard 10 Premium Ethylcellulose

Chemical Name:Ethylcellulose
CAS Number:9004-57-3
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, 1,4-Dioxane-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, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, APE-free, Hormones-free, Zero Calorie, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Naturally Derived, PFAS-Free, Mycotoxins-free, PAH-free, Aflatoxin-free, Formaldehyde-free, Plant-Based, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, FDA 21 CFR 163, Clean Air Act (CAA) Certified, Halal, British Pharmacopeia (BP), 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, FDA 21 CFR 172.868, CFDA Compliant (China), 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, FCC Compliant, Turkish RoHS Regulation, EU Cosmetic Regulation 1223/2009 Compliant, Regulation (EC) No. 1333/2008, Chinese Pharmacopeia (ChP), FDA 21 CFR 73.1, FDA 21 CFR 73.1001, FDA Compliant, Regulation (EU) No. 231/2012, FDA 21 CFR 573.420, ICH Q3C, Canadian Environmental Protection Act (CEPA), National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Directive 2023/915/EU, Belgian Law And Codex Alimentarius Standards, ICH Q3D
Manufacturing Technology:Tablet Coating, Granulation, Hot Melt Extrusion, Direct Compression, Encapsulation

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.

IFF Pharma SolutionsAvicel® PH - 113

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Tablets
Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-free, Endocrine Disruptor-free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, 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, Latex-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, Heavy Metal-free, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, FDA Compliant, Regulation (EU) No. 231/2012, ICH Q3C, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS)
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

Avicel® PH - 113 composed of microcrystalline cellulose, finds application in tablet formulations. Manufactured using direct compression, dry granulation, and wet granulation techniques, it serves as a binder and compression aid. Derived from non-animal sources, it meets pharmaceutical and nutraceutical standards.

IFF Pharma SolutionsPOLYOX™ WSR - 205 NF Grade

Chemical Name:Polyethylene Oxide
CAS Number:25322-68-3
Dosage Form:Gels, Osmotic Pump Tablet, Abuse Deterrent Tablets & Capsules, Tablets
Labeling Claims:Plant-Based, Residual Solvent -Free, Halal, Chlorine-free, Ethylene Glycol-free, Not Tested on Animals, Kosher, Allergen-free, No Added Formaldehyde, Vegetarian, Vegan, Nitrosamines-free, Naturally Derived, Heavy Metal-free, Not Listed In California Proposition 65, Diethylene Glycol-free
Certifications & Compliance:Japan Pharmacopeia (JP), US DMF, European Pharmacopeia (Ph. Eur.), Belgian Law And Codex Alimentarius Standards, ICH Q3D, Halal, Japan DMF, British Pharmacopeia (BP), Chinese Pharmacopeia (ChP), Kosher, Clean Water Act (CWA) Certified, EXCiPACT, CFDA Compliant (China), ICH Q3C, GMP, United States Pharmacopeia (USP), National Formulary (NF)
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.

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.

IFF Pharma SolutionsManucol® LB

Chemical Name:Sodium Alginate
Labeling Claims:Odor-free, Dioxin-free, Gold-Free, Phthalates-free, Cadmium-free, Kosher, Colorants-free, Endocrine Disruptor-free, PHO (Partially Hydrogenated Oil)-Free, Dye Free, Antibiotics-free, Palm Oil-free, Sugar-free, PVC-free, Aluminum-free, Pesticide-free, Paraben-free, Triphenyl Tin Compounds-Free, Copper-free, Plasticizer-free, Monosodium Glutamate (MSG)-free, Generally Recognized As Safe (GRAS), Caffeine Free, Preservative-free, Glycerin-free, Bisphenol A-free, Barium-free, APE-free, Hormones-free, GMO-free, Natural Latex Rubber-Free, Nitrosamines-free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free, Mercury-Free, Cobalt-free
Certifications & Compliance:British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, Doping-Free, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), EU Cosmetic Regulation 1223/2009 Compliant, IFRA Compliant, Chinese Pharmacopeia (ChP), FDA Compliant, Regulation (EU) No. 231/2012, National Formulary (NF), Japan Pharmacopeia (JP), Belgian Law And Codex Alimentarius Standards
Chemical Inventories:PICCS (Phillipines), AICS (Australia), KECI (Korea), ENCS (Japan), IECSC (China), NDSL (Canada), DSL (Canada)

Manucol® LB containing sodium alginate, is a versatile ingredient known for its antacid properties. It also acts as a controlled release agent, gelling agent, stabilizer, and thickener in pharmaceutical and nutraceutical formulations.

IFF Pharma SolutionsAvicel® PH - 103

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Dosage Form:Granules, Suspension, Tablets
Labeling Claims:Fragrance allergen-free, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dye Free, Herbicide-free, TSE-free, PFOA-free, Antibiotics-free, Bisphenol Derivatives-free, Palm Oil-free, Sugar-free, PVC-free, Diethylene Glycol-free, Gluten-free, Aluminum-free, Pesticide-free, Paraben-free, Halal, CMR Substances-free, Dioxane-free, Plasticizer-free, Ethylene Glycol-free, Monosodium Glutamate (MSG)-free, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Potassium-free
Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Kosher, EXCiPACT, United States Pharmacopeia (USP), European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, FDA 21 CFR 117, Nagoya Compliant, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), Belgian Law And Codex Alimentarius Standards
Manufacturing Technology:Dry Granulation, Wet Granulation, Direct Compression

Avicel® PH - 103 is a microcrystalline cellulose used in direct compression, dry granulation, and wet granulation technologies. It serves the healthcare and pharma markets, particularly in oral drug delivery and care solutions. This product is available in granule form.

IFF Pharma SolutionsLattice® NT-50

Chemical Name:Cellulose, Microcrystalline
CAS Number:9004-34-6
Functions:Binder
Labeling Claims:PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Dye Free, Pesticide-free, Allergen-free, Aluminum-free, Natural Latex Rubber-Free, Kosher, PFAS-Free, Preservative-free, PFOS-free, Halal, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Not Listed In California Proposition 65, Hormones-free, Sugar-free, Tributyl Tin Compounds-Free, Antibiotics-free, BSE-free, PVC-free, PAH-free, Phthalates-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, Plasticizer-free, APE-free, Latex-free, Non-GMO
Certifications & Compliance:ICH Q3C, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), cGMP, Generally Recognized As Safe (GRAS), Comprehensive Environmental Response, Compensations & Liability Act (CERCLA), Clean Water Act (CWA) Certified

Lattice® NT-50 an off-white product, is available as granules and tablets. It's caffeine-free, colorant-free, dioxin-free, and dye-free, meeting diverse preferences. A trusted binder in pharmaceutical and nutraceutical applications, it's provided in powder form for easy use.

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