GMP Certified / Ciprofloxacin Lactate and Sodium Chloride Injection

• Quality Standard: Bp, USP
• Ctd Dossier: Ready
• Documentation: Copp, COA
• Factory Certification: GMP
• Transport Package: Carton
• Specification: 100ml
• Model NO.: injection
• Trademark: Sinolead
• Origin: China
• Production Capacity: 100, 000, 000 Per Year

Product Description

 

Generic Name	Ciprofloxacin Lactate and Sodium Chloride Injection
Strength	100ml
Packing	1 bottle / box
Origin	China

Value-added services:
 Packaging design by our team
 Registration service by our team
 Registration dossier available by our team
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Product name:
Ciprofloxacin Lactate and Sodium Chloride Injection

Character:
This product is colorless or almost colorless clear liquid.

Indications:
For simple and complex infections caused by ciprofloxacin-sensitive pathogens. When intravenous administration is beneficial to the patient:
Urinary tract infections - mild, moderate, severe and concurrent infections, applicable to the following pathogens: Escherichia coli (including secondary bacteremia), Klebsiella pneumoniae subspecies pneumonia, Enterobacter clovis, Serratia marcescens, Proteus mirabilis, Pluffetenella reggii. Morgan Bacillus, citrobacter Divos, citrobacter Fraudiensis, Pseudomonas aeruginosa, Staphylococcus epidermidis or Enterobacter faecalis.
Lower respiratory tract infection - Mild to moderate infection for the following causes: E. coli, Klebsiella pneumoniae subspecies pneumonia, Enterobacter cloacae, Proteus mirabilis, Pseudomonas aeruginosa, Haemophilus influenzae and Haemophilus parainfluenza, and Streptococcus pneumoniae.
Skin and soft tissue infections - Mild to moderate infections for the following causes: Escherichia coli, Klebsiella pneumoniae subspecies pneumonia, Enterobacter cloacae, Proteus Mirabilis, Proteus vulgaris, Pruffeella stuartii, Bacillus morgana, Citrobacter Fredii, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus epidermidis, and Streptococcus pyogenes.
Bone and joint infections - mild to moderate infections, suitable for infections caused by Enterobacter cloacae, Serratia marcescens and Pseudomonas aeruginosa.
If the infection may be caused by anaerobic bacteria, appropriate treatment should be taken.
In order to isolate and identify the bacteria causing the infection and determine their sensitivity to Siproxacin ®, appropriate bacterial cultures and susceptibility tests should be performed. The results of these trials may be treated with Siproxacin ® by intravenous drip until the results are reported, and the most appropriate treatment should be used once the results are clear.
Similar to other drugs, some strains of P. aeruginosa can rapidly develop resistance when treated with Siproxacin ®, so regular bacterial culture and susceptibility testing during treatment can not only understand the antibacterial effect, but also obtain information about the potential for resistance.
Inhalation anthrax in adults and children (post-exposure) : Reduces the incidence of disease after inhalation of atomized anthrax bacilli and delays disease progression.
specification

Drug overdoes: 
If acute, large doses of oral overdoses occur, reversible nephrotoxicity may occur in some cases. Therefore, in addition to the usual emergency measures, it is recommended to monitor kidney function and take antacids containing magnesium and calcium to reduce the absorption of ciprofloxacin.
Only small amounts of ciprofloxacin after hemodialysis or peritoneal dialysis (< 10%) is cleared from the body.


Storage:
Ciprofloxacin is sensitive to light and should be used immediately after the injection bottle is removed from the box. Under light conditions, the undiluted solution remained fully effective for 3 days.
The solution will precipitate when stored at low temperature, and will disappear when restored to normal temperature. Therefore, storage in the refrigerator is not recommended.
Keep medicines out of reach of children.
Do not use after the expiration date.