USP40 Grade Chondroitin Sulfate Sodium Powder With 90% Purity for Arthritis
Chondroitin Sulfate Sodium 90% is a popular dietary supplement ingredient for joint care products. It is extracted from cartilages of health animals such as Avian, bovine,porcine or shark. It is also commonly used in combination with other joint care ingredients such as Glucosamine, Collagen, and shark cartilage powder.
As one of the first chondroitin suflate manufacturers in china, Jiaxing Hengjie Biopharmaceutical Co., ltd was founded in 1997 and had specialized in production and supply of chondroitin sulfate ever since.
Our chondroitin sulfate are up to USP,EP,BP,JP,CP and even customized standards with various origins available including bovine, porcine, Marine fish and avian. Our capacity of production is estimated to be 40MT per month. With outstanding quality of our products, we had gained a good reputation worldwide.
Please see below specification sheet:
Report Date Quantity:
SPECIFICATIONS (TEST METHOD)
White to off-white powder
|Identification||Infra Red Confirmed (USP197K)||Pass|
|Sodium reaction (USP191)||Positive|
|Loss on drying||Less than10%(USP731)||8.8%|
|Heavy Metal||NMT20PPM (MethodIIUSP231)||Pass|
|PH (1%H2O solution)||5.5-7.5(USP791)||6.2|
|Specific Rotation||- 20°~ -30°(USP781S)||-25.1°|
|Residue on Ignition||20%-30%(USP281)||23.5%|
|Clarity (5%H2O solution)||<0.35@420nm||0.17|
Total Bacteria Count
Yeast & Mold
|Staphylococcus Aureus||Negative (USP2022)||Negative|
|Particle size||100% through 80 mesh||Pass|
Storage: keep in an airtight container, protected from light.
Following is the quality management system of our company, according to the time:
2008-- A GMP workshop (300,000 clean class) was built and put into service. It was upgraded to 100,000 clean class in 2011
2010 May -- Received the Drug Manufacturing License issued by the State FDA. It was renewed on Sep 2, 2019 and valid until Sep 1, 2024
2010 October --ISO9001 & ISO 22000 Verified. It was renewed on Oct.11, 2018 and valid until October 11, 2021.
2012 April --Pass the FDA site inspection with zero inspectional observation
2012August --Received the NSF-GMP certificate and listed as a GMP manufacturer of dietary supplements on NSF website and renew the certificate every year.
2012 September--- Register our plant at EU Commission as an animal by products manufacture, the approval number is 3300DZ0091
2012 December –DMF NO. of Chondroitin Sulfate received from USFDA: 26474.
2014 March--- MSC Verified for Shark Chondroitin and Shark Cartilage Powder. It was renewed on March 2, 2017 and valid until March 1, 2020.
2016 March---HALAL Verified. It was renewed on March 30, 2016 and valid until March 29, 2021.
2018 March---Obtain Certificate of Recording for Export Food Manufacturing Enterprises and valid until March 2023
2019 June--- Obtain API registration number Y20190000453
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