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IFF Pharma Solutions
Avicel® 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 Solutions
Accelerate® 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 Solutions
Accelerate® DS - 813
Chemical Name:
Cellulose Gum
Functions:
Disintegrant
Manufacturing Technology:
Wet Granulation
Labeling Claims:
PHO (Partially Hydrogenated Oil)-Free, Monosodium Glutamate (MSG)-free, Colorants-free, Paraben-free, Vegan, Dye Free, Pesticide-free, GMO-free, Allergen-free, Aluminum-free, Generally Recognized As Safe (GRAS), Natural Latex Rubber-Free, PFAS-Free, Preservative-free, PFOS-free, Nanomaterials-free, Dioxin-free, Perfluorooctanoic Acid-free, Bisphenol A-free, Not Listed In California Proposition 65, Palm Oil-free, Hormones-free, Melamine-free, Endocrine Disruptor-free, Sugar-free, Tributyl Tin Compounds-Free, Antibiotics-free, Glycerin-free, BSE-free, PVC-free, PAH-free, Phthalates-free, Triphenyl Tin Compounds-Free, Caffeine Free, TSE-free, Plasticizer-free, APE-free, Ethylene Oxide-free, Non-GMO, Vegetarian
Certifications & Compliance:
Regulation (EU) No. 231/2012, ICH Q3C, European Pharmacopeia (Ph. Eur.), Nagoya Compliant, FDA 21 CFR Regulations, FDA Food Safety Modernization Act (FSMA), United States Pharmacopeia (USP), Regulation (EU) No. 1272/2008, cGMP, Japan Pharmacopeia (JP), Generally Recognized As Safe (GRAS), European Regulation 396/2005/EC, Doping-Free
Accelerate® DS - 813 is available in various dosage forms, including capsules, granules, and orally disintegrating tablets (ODTs). Manufactured using wet granulation technology, it serves as a disintegrant in pharmaceutical and nutraceutical formulations. It is supplied in powder form for ease of processing and formulation.