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Book Description Condition: New. PRINT ON DEMAND Book; New; Fast Shipping from the UK. No. book. Seller Inventory # ria9783639518610_lsuk
Book Description Condition: New. Seller Inventory # ABLING22Oct2817100460280
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Book Description Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Newly developed and validated reverse phase high performance liquid chromatography (RP-HPLC) method for the quantitative analysis of dexibuprofen. We could also develop and validate stability indicating RP-HPLC methods for dexibuprofen. RP-HPLC method was developed for the determination of dexibuprofen in single dosage forms. Stability indicating RP-HPLC methods were also developed for the determination of dexibuprofen in single dosage forms. Forced degradation study of dexibuprofen was carried out under acidic, alkaline, oxidative, dry heat and photostability conditions. Newly developed stability indicating RP-HPLC method was successfully applied to determine the drugs content from the pharmaceutical dosage forms in presence of their degradation products. This proposed method was validated as per ICH guidelines and can be applied successfully in routine analysis for quantitative analysis of dexibuprofen in single dosage forms without interference from commonly used excipients and additives. 68 pp. Englisch. Seller Inventory # 9783639518610
Book Description PAP. Condition: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000. Seller Inventory # L0-9783639518610
Book Description Taschenbuch. Condition: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Newly developed and validated reverse phase high performance liquid chromatography (RP-HPLC) method for the quantitative analysis of dexibuprofen. We could also develop and validate stability indicating RP-HPLC methods for dexibuprofen. RP-HPLC method was developed for the determination of dexibuprofen in single dosage forms. Stability indicating RP-HPLC methods were also developed for the determination of dexibuprofen in single dosage forms. Forced degradation study of dexibuprofen was carried out under acidic, alkaline, oxidative, dry heat and photostability conditions. Newly developed stability indicating RP-HPLC method was successfully applied to determine the drugs content from the pharmaceutical dosage forms in presence of their degradation products. This proposed method was validated as per ICH guidelines and can be applied successfully in routine analysis for quantitative analysis of dexibuprofen in single dosage forms without interference from commonly used excipients and additives. Seller Inventory # 9783639518610
Book Description Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Modi Meghal V.Meghal V. Modi, Assistant Professor, Department of Quality Assurance at B.S. Patel Pharmacy College, Saffrony Institute of Technology At-Post Linch, Dist-Mehsana affiliated to Gujarat Technological University, Ahmedaba. Seller Inventory # 4993409