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Development and validation of RP-HPLC method for determination of acetazolamide, furosemide and phenytoin extemporaneous suspensions 被引量:1
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作者 warisada sila-on Salinee Na-Ranong +2 位作者 Sirilak Rakrod Sarote Ornlaor Zongporn Joungmunkong 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2016年第1期138-139,共2页
The development of the extemporaneous preparations allows physicians to adjust the dose for pediatric patients and provides for a more convenient dosage vehicle for those patients with difficulty swallowing tablets[1]... The development of the extemporaneous preparations allows physicians to adjust the dose for pediatric patients and provides for a more convenient dosage vehicle for those patients with difficulty swallowing tablets[1].As such,the production unit of pharmacy division,Sappasit Prasong Hospital,Ubon Ratchathani province,prepared the extemporaneous formulations such as Acetazolamide(AM),Furosemide(FM)and Phenytoin(PT)powder for suspensions.The extemporaneous suspensions of 10 mg/mL AM,2 mg/mL FM and 10 mg/mL PT were prepared from 250 mg Diamox?,40 mg Lasix?and 50 mg Dilantin?tablets,respectively and diluted with syrup vehicle. 展开更多
关键词 DEVELOPMENT and VALIDATION of RPHPLC method Extemporaneous SUSPENSIONS
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