C - Chemistry – Metallurgy – 07 – D
Patent
C - Chemistry, Metallurgy
07
D
260/109
C07D 501/36 (2006.01) A61K 31/545 (2006.01)
Patent
CA 1097341
Abstract of the Disclosure Essentially crystalline cefazolin sodium (7- (1-(1H)-tetrazolylacetamido)-3-[2-(5-methyl-1,3,4-thia- diazolyl)thiomethyl]-3-cephem-4-carboxylic acid, sodium salt, a standard antibiotic) for parenteral administration is prepared by a freeze-drying process wherein an ethanol- water solution of cefazolin sodium is chilled slowly from room temperature to -10°C. over a 3-12 hour-period, and then rapidly cooled until the mixture is completely solidified before subjecting said frozen solution to a high vacuum and a moderate amount of heat to sublime the frozen solvent therefrom. The resulting powder dissolves rapidly in accept- able pharmaceutical diluents. X-4494
291616
Bornstein Michael
Cise Michael D.
Eli Lilly And Company
Gowling Lafleur Henderson Llp
LandOfFree
Method of preparing a rapidly dissolving powder of sterile... does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Method of preparing a rapidly dissolving powder of sterile..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method of preparing a rapidly dissolving powder of sterile... will most certainly appreciate the feedback.
Profile ID: LFCA-PAI-O-1050333