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Chondroitin Sulphate Sodium
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| Place of Origin | Zhejiang Province, China |
| Brand Name | HS |
| Certification | NSF-GMP,ISO9001/22000,DMF,HALAL |
| Model Number | USP41 Grade 90% |
USP41 Grade Chondroitin Sulphate Sodium Extracted From Pure Bovine Cartilages For Arthritis
Our company Jiaxing Hengjie Biopharmaceutical Co.,ltd. is a GMP manufacturer of chondroitin sulfate sodium from bovine cartilage with purity of 90% by CPC titration.
Chondroitin Sulfate sodium is a type of mucopolysaccharides extracted from cartilages of health animals for human consumption. This one is extacted from bovine cartilage. It is very good for Joint health and Osteoarthritis.
Chondroitin sulfate could be produced into Tablets, Capsules, Sachets or even creams.
We are also able to supply other joint care ingredients including glucosamine, shark cartilage powder, and collagen. We can ship all the joint health ingredients together for you to save your time and money.
Specifications:
|
ITEMS |
SPECIFICATIONS |
TEST METHOD |
|
Appearance |
White to off-white powder |
Visual checking |
|
Identification |
Infra Red Confirmed |
(USP197K) |
|
|
Sodium reaction |
(USP191) |
|
Assay(ODB) |
NLT90% |
(CPC Titration) |
|
Loss on drying |
Less than10% |
(USP731) |
|
Protein |
NMT6.0% |
(USP41) |
|
Heavy Metal |
NMT20PPM |
(Method I USP231) |
|
PH (1%H2O solution) |
5.5-7.5 |
(USP791) |
|
Specific Rotation |
- 20°~ -30° |
(USP781S) |
|
Residue on Ignition |
20%-30% |
(dry base)(USP281) |
|
Organic Volatile Residual |
NMT0.5% |
(USP467) |
|
Clarity (5%H2O solution) |
<0.35@420nm |
USP41 |
|
Electrophoretic purity |
NMT2.0% |
(USP726) |
|
Total Bacteria Count |
<1000CFU/g |
(USP2021) |
|
Yeast & Mold |
<100CFU/g |
(USP2021) |
|
Salmonella |
Negative |
(USP2022) |
|
E.Coli |
Negative |
(USP2022) |
|
Staphylococcus Aureus |
Negative |
(USP2022) |
|
Particle size |
100% through 80 mesh |
Pass |
Applications:
The most common use of Bovine chondroitin sulfate sodium is to produce joint health dietary supplements in combination with Glucosamine and MSM(Methyl-Sulfonyl-Methane) in Tablets. It could also be used to produce capsules and powders in sachets together with glucosamine and MSM.
People suffering from arthralgia, articular pain or stiff joints Glucosamine Sulfate .
People suffering from arthritis or muscle inflammation.
People desiring to prevent arthropathies or caput femoris necrosis.
People suffering from scapulohumeral periarthritis, cervical spondylosis, rheumatoid disease, rheumatalgia, hyperosteogeny and sciatica.
Quality Management System
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 October 22, 2014 and valid until Sep 1, 2024
2010 October --ISO9001 & ISO 22000 Verified. It was renewed on Oct.11, 2018 and valid until Oct11, 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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