• Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
  • Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
  • Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
  • Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
  • Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
  • Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate

Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate

Varieties: Other
Component: Chemical Synthetic Drugs
Type: Other
Pharmacodynamic Influential Factors: Other
Storage Method: Prevent Exceeding Quality Guarantee Period
Veterinary Reg. No.: Other
Customization:

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Basic Info.

Model NO.
Ceftazidime Pentahydrate+Sodium Carbonate
CAS No
78439-06-2
Mf
C19h18n5nao7s3
Appearance
White Crystal Powder
Grade Standard
Medicine Grade
Shelf Life
2 Years
Transport Package
Bag, Carton, Drum
Specification
25kg/drum
Trademark
Arshine
Origin
China
Production Capacity
200 Tons/Year

Product Description

pharmaceutical intermediate Ceftazidime Pentahydrate+Sodium Carbonate
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 Ceftiofur sodium is the sodium salt of ceftiofur, which belongs to the third generation cephalosporin antibiotics, Chemical properties are stabie, appearance is light yellow to white crystalline powder, aqueous solution has a shorter retention time, it should be diluted into a solution before use.It is used for the treatment of respiratory disease of sheep,horses, cattle, pigs (pleuropneumonia),and the treatment of pets, day-old broiler infectious diseases.
Function
 Ceftiofur sodium is mainly used for serious infection of bacteria and Escherichia coli and Salmonella in poultry.
1. High temperature and high fever caused by systemic or local infection of viruses and bacteria, coughing, gasping, difficulty in breathing, redness and purpleness of the skin, purple hair in the ears, ulceration of the mouth and hoof, abortion of abortion, circling, hind limb paralysis, no food, no lying Start, constipation and diarrhea.
2, infectious pleurisy, actinomycetes, Pasteurella multocida, Streptococcus mutans, piglet yellow and white peony, Salmonella, Haemophilus parasuis, atrophic rhinitis, chlamydia and so on.
3, livestock prenatal and postpartum high fever, endometritis, mastitis, no milk and less milk syndrome, laminitis, rot rot, bovine bacillus, transport fever, pneumonia, nasal atrophy, etc.

Application 
Ceftiofur sodium is a veterinary clinical special antibiotic for cephalosporins and is a broad-spectrum antibacterial. It has strong antibacterial activity against Gram-positive bacteria and Gram-negative bacteria. Ceftiofur acts on the transcriptional peptidase to block the synthesis of the peptide, and the bacterial cell wall is deleted to achieve bactericidal action. Ceftiofur has a stable β-lactam ring and is not easily destroyed by drug-resistant bacteria. It can act on Gram-positive and Gram-negative bacteria producing β-lactamase.
Ceftiofur sodium is a compound preparation for bactericidal, anti-inflammatory, antipyretic and analgesic. Ceftiofur sodium is a third-generation cephalosporin antibiotic for veterinary clinics. It has a broad-spectrum and high-efficiency bactericidal effect. For G+ and G-bacteria, including β- The strains of lactamy mildew have a strong killing effect, and ceftiofur sodium absorbs rapidly after muscle and subcutaneous injection, reaching an effective peak concentration of 0.5-0.3 hours. It is widely distributed throughout the body and is the best new drug for clinical treatment of bacterial diseases.
TEST SPECIFICATION RESULT
Character White or grayish yellow powder,odor free and humidifying Conform
Identification 1. In the chromatogram of the assay, the retention time of the principal peak in the chromatogram obtained with the test solution corresponds to that of the principal peak in the chromatogram obtained with reference solution
2. It gives flame reaction of sodium salt
Conform
Water Not more than 3.0% 0.71%
Acidity(pH) 5.5~7.5 6.2
Color of solution No more intensity colored than reference solution Yedllow 9 or Orange-yellow 9 Less intensely colored than reference solution Yellow 8
Clarity of solution No more pronounced than that of reference suspension I Less pronounced than that of reference suspension I
Assay (Ceftiofur sodium) No less than 98.0%(anhydrous and acetoe free) 98.8%
Related substances Biggest individual impurity No more than 0.5% 0.1%
Total No more than 3.0% 0.98%
Residual solvents Acetoe: no more than 2.0% 1.0%
Particulate matter ≥10μm:no more than 5000 particles/g 597 particles/g
≥25μm:no more than 500 particles/g 27 particles/g
Bacterial endotoxin No more than 0.2EU/mg (Ceftiofur) Less than 0.20EU/mg(Ceftiofur)
Sterility No growth of micro-organisms should occur after 14 days of incubation No growth of micro-organisms should occur after 14 days of incubation
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 

Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate

Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
Pharmaceutical Intermediate Ceftazidime Pentahydrate+Sodium Carbonate
 
 

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Registered Capital
30000000 RMB
Management System Certification
ISO 9001, GMP, HACCP