Injectable Hyaluronic Acid Powder EP7.0 Pharmaceutical Grade For
What is pharma grade sodium hyaluronic acid ?
Hyaluronic acid (HA) is a straight chain macromolecular
mucopolysaccharide composed Of repeat disaccharide units of
glucuronic acid and N-acetylglucosamine. The commercial HA is
commonly a sodium salt, called sodium hyaluronate, habitually
called hyaluronic acid. Its molecular weight is from several ten
thousand to several million. It's aqueous solution has outstanding
moisture keeping ability, high viscoelasticity and lubricity. It is
widely used in cosmetics, pharmacy and health and beauty food.
Pharmaceutical Grade sodium Hyaluronic acid is the sodium
hyaluronate utilized as a part of medications. This is an oral
evaluation utilized for parenteral arrangements, yet excluding
intra-articular and intra-visual preparations.It is typically
utilized as a part of the oral or topical outside medications, for
example, the blaze salve, oral tablet.
The detailed specification of Pharma Grade sodium hyaluronic acid:
|EP 7.0, Pharma Grade|
|For the production of oral or parenteral preparations, not
including intra-articular and intra-ocular preparations|
|white or almost white powder or fibrous aggregate|
White or almost white powder or fibrous aggregateq
|A. Infrared Absorption||complies with the Ph. Eur. Reference spectrum of sodium hyaluronate|
B. Reaction of sodium
Apperance of solution
|A260nm ≤ 0.5|
|≤ 10 PPM|
Loss on drying
|Residual Solvents (Ethanol)|
What is the Application of pharmaceutical Grade Sodium Hyaluronic
Injectable Grade sodium hyaluronic corrosive is utilized as a part
of the Ophthalmic viscosurgical devices,Intra-articular infusion,
Anti-cement items or dermal filler. It is utilized as a part of
medicinal applications in various capacities, for example, to
decrease irritation, ease the torment in joints or reestablish the
liquids, and ensure against the breakdown of ligaments.
The type of pharmaceutical items that containing sodium hyaluronate
1. Ophthalmic viscosurgical gadgets
2. Intra-articular infusion
3. Hostile to cement items
4. dermal filler
What is the advantage of our company:
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
October 21, 2019
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
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:
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,
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