Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc

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Powder: Yes
Customized: Customized
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  • Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
  • Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
  • Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
  • Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
  • Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
  • Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
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Basic Info.

Model NO.
cellulose
Suitable for
Adult
State
Solid
Purity
>99%
Product Name
Clavulanate
Transport Package
Drum
Specification
99%
Trademark
HS
Origin
China
HS Code
2904201000
Production Capacity
100000

Product Description

Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc
Name of product Amoxicillin and Clavulanate postassium(4:1)
Tests  Specifications  Results
Characters A white to slightly yellow powder .hygroscopic A white powder , hygroscopic
Identification The retention time of the two major peak in the chromatogram of the Assay preparation corresponds to that exhibited in the chromatogram of the standard preparation. Conforms
Water 9.0% ~12.0% 10.2%
PH 3.5~7.5 5.3
Related substances Any impurity ≤2.0% (calculated on the basis of amoxicillin peak areas in the chromatogram of reference solution) 0.03%
Total impurities ≤5.0% (calculated on the basis of amoxicillin peak areas in the chromatogram of reference solution) 0.06%
Assay Amoxicillin(C16 H19 N3 O5S)≥695 μg/mg, Amoxicillin 772 μg/mg
Clavulanic acid(C8 H9 NO5) ≥ 176μg/mg, Clavulanic acid 193 μg/mg
The ratio of Amoxicillin to Clavulanic acid should be 3.6~ 4.4 4.0
 
Name of product Amoxicillin and Clavulanate postassium(7:1)
If you need 7:1, please contact our customer service
Name of product Clavulanate Potassium-Microcrystalline Cellulose(1:1)
Tests  Specifications  Results
Appearance White or almost white powder, hygroscopic Almost white powder, hygroscopic
Identification (l)HPLC: positive Positive
(2) Reaction (b) of potassium: positive Positive
(3) Reaction of cellulose: positive Positive
pH 4.8 - 8.0 5.7
Polymeric impurities and other impurities absorbing at 278 nm NMT 0.40 0.033
Water NMT2.5% 0.46%
Related substances Impurity E: NMT 1.0% 0.014%
Impurity G: NMT 1.0% 0.0017%
Any other single impurity (major): NMT 0.10% <0.05%
Total impurities: NMT 2.0% 0.016%
Assay (HPLC) 91.2% ~107.1% (as content of potassium clavulanate stated on the label) 100.4%
CLAV.ACID(as is)38.3%~45.0% 42.1%
CLAV. POT. (as is)45.6%~53.5% 50.2%
Conclusion Conforms to the requirements of EP.
Name of product Clavulanate Potassium-Silicon Dioxide(1:1)
Tests  Specifications  Results
Appearance A white or almost white powder, hygroscopic A  white powder, hygroscopic
Identification (1) The principal peak in the chromatogram obtained with the test solution is similar in retention time to the principal peak in the chromatogram obtained with reference solution (a). Conforms
(2)lt gives reaction (b) of potassium. Conforms
(3) It gives the reaction of silicates Conforms
PH 4.8 ~8.0 5.1
Absorbance ≤0.40(278nm) 0.064
Related substances Impurity E≤1.0% 0.09%
Impurity G≤1.0% <Reporting      threshold limit0.05%
Any other impurity ≤ 0.2% <Reporting      threshold limit0.05%
Total impurities≤ 2.0% 0.09%
water ≤2.5% 0.53%
Residual Solvents Acetone≤5000ppm 48ppm
1-butanol≤5000ppm 909ppm
Assay It contains Potassium Clavulanate(C8H8KNO5)48.0%~53.5%,calculated on the anhydrous basis. 49.9%
Conclusion The results conform with EP and Enterprise standard.

Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc

What is Amoxicillin?

 
Amoxicillin water soluble powder is white crystall powder, odourless, taste bitter. This product in DMF dissolve easily in the dissolved in methanol in slightly soluble in glacial acetic acid in water or chloroform micro dissolve.
Suitable for various kinds of various infections caused by sensitive bacteria.
 

Function of Amoxicillin

1. hemolytic streptococcus, Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, or due to otitis media, sinusitis, pharyngitis, tonsillitis and other upper respiratory tract infection
2. Escherichia coli, Enterococcus faecalis, Proteus mirabilis, or urogenital tract infection caused by
3. hemolytic Streptococcus, Staphylococcus, or Escherichia coli-induced skin and soft tissue infections
4. hemolytic streptococcus, Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, or with acute bronchitis, pneumonia and other lower respiratory tract infection
5. acute simple gonorrhea
6. for the treatment of typhoid and other Salmonella infections, typhoid fever and carriers of leptospirosis; amoxicillin and clarithromycin may, lansoprazole triple drug eradication of the stomach, duodenum, Helicobacter pylori, Reduce the recurrence rate of peptic ulcer.
 

Application of Amoxicillin

1. Amoxicillin water soluble powder can be used as a broad-spectrum semisynthetic penicillin.
2. Amoxicillin water soluble powder is used to treat tonsillitis,laryngitis, pneumonia,chronic bronchitis,urinary tract infection,skin soft tissue infection,pyogenic pleuritis,liver and gallbladder infection,septicaemia,typhoid,dysentery and so on.
3. Amoxicillin water soluble powder is antiseptic drug,and its effect and application are similar to benzylpenicillin. The advantage is that the serum protein binding rate is low and the blood concentration is more than two times higher than ampicillin.
4. Amoxicillin water soluble powder is a safe,effective and effective drug. It was developed by Beecham (Beecham) in 1968.
5. Amoxicillin water soluble powder is a broad-spectrum semi synthetic penicillin antibacterial agent.Its antibacterial mechanism is to interfere with the synthesis of the cell wall of sensitive bacteria,inhibit the metabolic enzymes of bacteria,trigger the activity of autolysis enzyme of bacteria itself,make bacteria swollen,deform and break up and dissolve death.

How should I take amoxicillin and clavulanate potassium?

Take amoxicillin and clavulanate exactly as prescribed by your doctor. Follow all directions on your prescription label. Do not take this medicine in larger or smaller amounts or for longer than recommended.

Take the medicine every 12 hours, at the start of a meal to reduce stomach upset.

Do not crush or chew the extended-release tablet. Swallow the pill whole, or break the pill in half and take both halves one at a time. If you have trouble swallowing a whole or half pill, talk with your doctor about using another form of amoxicillin and clavulanate potassium.

The chewable tablet must be chewed before you swallow it.

Shake the liquid medicine well just before you measure a dose. Measure liquid medicine with the dosing syringe provided, or with a special dose-measuring spoon or medicine cup. If you do not have a dose-measuring device, ask your pharmacist for one.

Use this medicine for the full prescribed length of time. Your symptoms may improve before the infection is completely cleared. Skipping doses may also increase your risk of further infection that is resistant to antibiotics. Amoxicillin and clavulanate potassium will not treat a viral infection such as the flu or a common cold.

This medicine can cause unusual results with certain lab tests for glucose (sugar) in the urine. Tell any doctor who treats you that you are using amoxicillin and clavulanate potassium.

Store the tablets at room temperature away from moisture and heat.

Store the liquid in the refrigerator. Throw away any unused liquid after 10 days.


Amoxicillin and clavulanate potassium is used to treat a variety of bacterial infections of the antibacterial agent , the amoxicillin and potassium clavulanate synthesis . It is divided into oral amoxicillin and clavulanate potassium tablets and intravenous dry suspension . 

Clavulanate Potassium Silicon Dioxide Microcrystalline Cellulose Mcc

Items

Specifications

Results

Characteristic

White or almost white
 powder 

Almost white powder

 

pH

3.5 ~ 6.0

4.5 

Crystallinity

Conforms 

Conforms 

Water

11.5% ~ 14.5%

12.8% 

Assay 

(on the anhydrous basis) 

900~1050 μg/mg 

981μg/mg 

Tapped density

≥0.70g/ml 

0.81g/ml 

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