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HDK® N20 P Pharma banner
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HDK® N20 P Pharma
  • Functions:Glidant, Flow Promoter
  • Chemical Name:Pyrogenic Silica
  • Labeling Claims:Animal Products-free, TSE-free, BSE-free, GMO-free, Non-GMO
  • Certifications & Compliance:Directive 2011/65/EC amended through EU/2015/863 (RoHS), Consumer Product Safety Improvement Act (CPSIA), Directive 2003/15/EC, FDA 21 CFR 178.3120, FDA 21 CFR 178.3570, EC No.1907/2006, FDA 21 CFR 175.350, FDA 21 CFR 175.105, BSE & TSE, Coalition of Northeastern Governors (CONEG), BfR 52 Recommendation , Directive 2010/75/EU, ISO 9001, European Pharmacopeia (Ph. Eur.), Directive 2001/83/EC, EC No. 1935/2004, FDA 21 CFR 182.90, National Formulary (NF), FDA 21 CFR 176.200, United States Pharmacopeia (USP), GB 9685-2016, FDA 21 CFR 177.2420, FDA 21 CFR 176.210, ISO 14001, Regulation (EU) No. 10/2011 (PIM), Hazard Analysis Critical Control Point (HACCP), FDA 21 CFR 176.170, BfR Recommendation, Directive 2000/53/EC, FDA 21 CFR 177.2600, FDA 21 CFR 176.180, Regulation (EU) No. 1169/2011, FDA 21 CFR 178.3297, FDA 21 CFR 177.1400, USP Class IV, FDA 21 CFR 177.1200, FDA 21 CFR 175.300, Generally Recognized As Safe (GRAS), FDA 21 CFR 175.390, Swiss Ordinance (SR 817.023.21), EU Packaging Directive (94/62/EC)
  • Dosage Form:Tablets, Powder & Powder Blends
  • Synonyms:Fumed Silica, Silica, Silicon Dioxide
HDK® N20 P Pharma is a synthetic, hydrophilic, amorphous silica powder produced via flame hydrolysis. It is a white, high-purity colloidal powder. This product serves as a glidant for tableting, effectively improving the flow of powders. Furthermore, HDK® N20 P Pharma undergoes testing according to the EP and USP/NF standards.

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