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IFF Pharma Solutions

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

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METHOCEL™ K200M Premium HPMC banner
IFF Pharma SolutionsMETHOCEL™ K200M Premium HPMC
  • Chemical Name:Hydroxypropyl Methylcellulose
  • CAS Number:9004-65-3
  • Dosage Form:Capsules, Suspension, Tablets
  • Labeling Claims:Low Odor, Odor-free, Quaternary Ammonium Salt-Free, BSE-free, Phthalates-free, Kosher, Endocrine Disruptor-free, Tributyltin (TBT) - Free, Allergen-free, PHO (Partially Hydrogenated Oil)-Free, Vegan, Dairy-free, Persistent Organic Pollutants (POP)-free, 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, Latex-free, APE-free, Hormones-free, Zero Calorie, Natural Latex Rubber-Free, PFOS-free, Non-GMO, PFAS-Free, Fungicide-free, PAH-free, Iodide-free, Pareve, Potassium-free
  • Certifications & Compliance:cGMP, Halal, British Pharmacopeia (BP), Waste Electrical & Electronic Equipment Directive (WEEE), FDA 21 CFR 172.874, Indian Pharmacopeia, FDA 21 CFR 176.170, FDA Food Safety Modernization Act (FSMA), Kosher, Swiss Ordinance (SR 817.023.21), EXCiPACT, FDA 21 CFR 175.300, United States Pharmacopeia (USP), FDA 21 CFR 174.5, Regulation (EU) No. 10/2011 (PIM), FSC Certified, European Pharmacopeia (Ph. Eur.), Chinese Pharmacopeia (ChP), FDA Compliant, ICH Q3C, GMP, Nagoya Compliant, FDA 21 CFR 175.105, National Formulary (NF), Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), FDA 21 CFR 176.180, Belgian Law And Codex Alimentarius Standards
  • Manufacturing Technology:Tablet Coating, Granulation
METHOCEL™ K200M Premium HPMC, identified as cellulose ethers and hypromellose, serves a wide array of functions across capsules, suspensions, tablets, granulation, and tablet coating applications. It acts as a binder, film former, gelling agent, mucoadhesive, solubilizer, thickener, and viscosity modifier. Notably, it is water-soluble, ensuring versatility and efficacy in formulations.
Avicel® DG banner
IFF Pharma SolutionsAvicel® DG
  • Chemical Name:Calcium Hydrogen Phosphate, Cellulose, Microcrystalline
  • CAS Number:9004-34-6
  • Dosage Form:Tablets
  • Labeling Claims:Dioxin-free, BSE-free, Phthalates-free, Kosher, Colorants-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, Caffeine Free, Preservative-free, Glycerin-free, Vegetarian, Bisphenol A-free, Ethylene Oxide-free, Latex-free, APE-free, Hormones-free, Natural Latex Rubber-Free, Perfluorooctanoic Acid-free, PFOS-free, Non-GMO, PFAS-Free, PAH-free, Tributyl Tin Compounds-Free
  • Certifications & Compliance:cGMP, British Pharmacopeia (BP), FDA Food Safety Modernization Act (FSMA), Regulation (EU) No. 1272/2008, Kosher, EXCiPACT, United States Pharmacopeia (USP), European Regulation 396/2005/EC, European Pharmacopeia (Ph. Eur.), Regulation (EU) No. 1169/2011, FCC 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® DG derived from non-animal sources, is a versatile powder used in tablet manufacturing. Its chemical composition includes calcium, hydrogen phosphate, cellulose, and cellulosics. Employing direct compression or wet granulation techniques, it functions as a binder and compression aid in tablet formulations.
Manucol® LMT banner
IFF Pharma SolutionsManucol® LMT
  • Chemical Name:Sodium Alginate
  • Labeling Claims: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, Not Listed In California Proposition 65, 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:TSCA (USA), PICCS (Phillipines), AICS (Australia), ENCS (Japan), IECSC (China), NDSL (Canada), DSL (Canada), ECL (Korea)
Manucol® LMT boasts a range of labeling claims, including being caffeine-free, colorant-free, dioxin-free, dye-free, hormone-free, and free of monosodium glutamate (MSG). In addition, it serves various functions in pharmaceuticals and nutraceuticals, acting as an antacid, controlled release agent, gelling agent, stabilizer, and thickener.

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