Diclofenac Sodium Powder Potent Antipyretic Analgesic Anti-inflammatory Drugs

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Diclofenac Sodium Specification

Nome do Produto:Diclofenac Sodium
CAS: 15307-79-6
Padrão: BP
Natural/Synthetic: Synthetic
Level: Pharmaceutical grade
Content: 99%
Aparência: white powder
Embalagem: 25KG/kraft paper bag
Category: Matérias-primas farmacêuticas
Industry: Pharmaceuticals
Field: potent antipyretic analgesic anti-inflammatory drugs
Deferred products: Diclofenac sodium enteric-coated tablets Suppositories Elixir Sustained release tablets Sustained release capsules
Use: Relieves rheumatoid arthritis, osteoarthritis. Acute spondyloargia, gouty arthritis, rheumatoid arthritis and other acute arthritis symptoms or persistent symptoms of joint swelling and pain
Usage and dosage: Adult human rheumatoid arthritis 150mg~200mg/day, divided into 2~4 times, gradually reduced to the minimum effective amount after reaching the therapeutic effect, usually 75mg~100mg/day, divided into 3 times; Osteoarthritis started 100mg~150mg/day, divided into 2~3 servings, gradually reduced to the minimum effective dose after reaching the curative effect; Ankylosing spondylitis started 100mg~125mg/day, divided into 4~5 times serving, gradually reduced to the minimum Effective amount; Children (age 1 and above) daily by weight 0.5mg ~ 2mg/kg, 2 para 3 times service.

 

Diclofenac Sodium Certificate of Analysis

Nome do Produto Diclofenac sodium
CAS. 15307-79-6 Embalagem exterior 25KG/drum
Data de produção 2017.05.30 Validade 2020.05.30
norma aprovada BP2010
Itens de análise Especificação Resultados
Aparência White or yellowish crystalline powder White crystal powder
Identificação A.IR infrared D. Identification of sodium salt Conforme
Solution appearance Clarify 0.5% methanol solution UV440nm not more than 0.05 Clear A=0.025
Substâncias relacionadas Impurity A: not more than 0.2 Single impurity: 0.08%
Impurity F Menos que 0.15% Conforme
Other non-specific impurities Menos que 0.1% Conforme
total de impurezas Menos que 0.4% 0.08%
Metal pesado Less than 10PPM Conforme
Perda ao secar Menos que 0.5% 0.31%
Ensaio 99.0-101.0% 99.66%
Conclusão Qualificado

 

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