High Quality Active Pharmaceutical Ingredients Diclofenac Sodium China

• Powder: Yes
• Customized: Customized
• Certification: GMP, HSE, ISO 9001, USP, BP
• Suitable for: Elderly, Children, Adult
• State: White Powder
• Purity: >99%
• Model NO.: Frazer-Diclofenac
• Storage: Cool Dry Place
• Active Ingredient: Diclofenac Sodium
• Grade Standard: Medicine Grade
• Shelf Life: 2 Years Proper Storage
• Application: Vertinary Raw Materials
• MOQ: 1kg
• MW: 240.75
• Mf: C14h10cl2nnao2
• Package: Aluminium Foil Bag and Carton
• Color: White Powder
• Transport Package: Foil Bag
• Specification: 99%
• Trademark: Xi′an Frazer Biotech Co., Ltd.
• Origin: China
• Production Capacity: 250kg/Month

Product Description

High Quality Active Pharmaceutical Ingredients Diclofenac Sodium China

Products Description 
Diclofenac sodium is a non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.

Diclofenac Sodium is the sodium salt form of diclofenac, a benzene acetic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with analgesic, antipyretic and anti-inflammatory activity. Diclofenac sodium is a non-selective reversible and competitive inhibitor of cyclooxygenase (COX), subsequently blocking the conversion of arachidonic acid into prostaglandin precursors. This leads to an inhibition of the formation of prostaglandins that are involved in pain, inflammation and fever.

Application of Diclofenac Sodium 

1. Acute and chronic rheumatoid arthritis, acute and chronic arthritis, acute and chronic ankylosing spondylitis, and osteoarthritis.
2. Periarthritis, bursitis, tendonitis and tenosynovitis.
3. Low back pain, sprains, strains and other soft tissue injuries.
4. Acute gout.
5. Dysmenorrhea or attachment inflammation, toothache and postoperative pain.

Function of Diclofenac Sodium

1. Treat inflammation and pain, mostly those associated with arthritis.
2. Post-traumatic pain and inflammation
3. Severe otolaryngological infection pain and inflammation (such as tonsillitis, otitis, sinusitis, etc.) should be combined with anti-infective drugs.

Specification

Items	Standard	Test Result
Appearance	White crystals or crystalline powder	White crystalline powder
Identification	Infrared absorption	Conform
Assay	98.5%~101.5%	99.3%
Residue on ignition	≤0.4%	<0.06%
Sulfate (SO4)	≤0.03%	<0.03%
Iron (Fe)	≤30ppm	<30ppm
Heavy metals (Pb)	≤15ppm	<15ppm
Related compounds	Not more than 0.5% of any individual impurity is found; Not more than 2.0% of total impurities is found	Conform
Specific rotation [α]D^25	+5.7°~+6.8°	+5.9°
Loss on drying	8.0~12.0%	11.1%
Conclusion	This batch is conforming with the standard of USP39.