• GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection
  • GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection
  • GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection
  • GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection
  • GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection
  • GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection

GMP Certified 0.5% Metronidazole Infusion & Metronidazole Injection

Application: Surgery
Usage Mode: For external use
Suitable for: Elderly, Children, Adult
State: Liquid
Shape: Injection
Type: Inorganic Chemicals
Samples:
US$ 100/Piece 1 Piece(Min.Order)
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Customization:
Gold Member Since 2005

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Rating: 5.0/5
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Basic Info.

Model NO.
MTDI
Pharmaceutical Technology
Chemical Synthesis
Drug Reg./Approval No.
Available
Drug Ad Approval No.
Available
Color
Transparent
Form
Liquid
GMP
Available
MSDS
Available
Transport Package
80bottle/Carton
Specification
100ml: 0.5g
Trademark
Fraken
Origin
China
HS Code
300490
Production Capacity
1million Bottles/Bags Per Month

Product Description

Metronidazole Injection

[Indications and Clinical use]: For treatment of anaerobe infection.
[Strength]: 250ml: 0.5g, 100ml: 0.5g
Structural formula: C6H9N3O3
Description
The product is colorless or almost colorless pellucid liquid.
Pharmacology and toxicity
The first one is the potent Anaerobicidal Nitro-imidazole derivative. The exact mechanism of action of metronidazole is unknown. At physiologic pH, metronidazole is un-ionized and taken up readily by anaerobic organisms. The medicine then undergoes intracellular chemical reduction via mechanisms unique to anaerobes. Reduced metronidazole interacts with DNA and inhibits nucleic acid synthesis, leading to cell death. Metronidazole is equally effective against dividing and nondividing cells.
Indications
This product is mainly used for the treatment of anaerobic bacteria infections.
Pharmacokinetics
The peak value is observed 20mins after administering by intravenous drip and binding rate with protein <5%. After absorption Metronidazole distributes widely in all kinds of tissues and body liquids, and pass easily blood brain barrier to the tissues such as saliva, placenta, bile, latex, ammiotic fluid, semen, urine, purulence, cerebrospinal fluid and etc. It is reported that the concentration in placenta, latex, bile is similar with that in plasma.
For the healthy people the concentration of Metronidazole in the cerebrospinal fluid is about 43% of that in the plasma, and the effective concentration can remain 12hours. 60~80% of the preparation is excreted via kidney, about 20% of Metronidazole is excreted unchanged in the urine, the other is excreted in the urine as the products of metabolism (25%-glucuronicacid combo, 14%-other kinds of products of metabolism). 10% of Metronidazole is excreted in the dejection, and 14% is excreted from skin.
Disease treated Metronidazole is mainly used in the treatment of anaerobe bacterial infection.
Administration and dosage by drip phleboclysis.
1. Doses for the adult In the treatment of anaerobic bacteria infections, administer by intravenous drip according to 1g/70kg for the first time, and calculate the does according to 7.5 mg/kg during the course of treatment, and interval time is 6~8 hours.
2. Doses for the children in the treatment of anaerobic bacteria infection, the doses are similar with that of the adult.
Side-effect 15~30% of the cases were reported side-effect, and adverse reactions frequently associated with Metronidazole include: Digestive tract reaction such as nausea, vomiting, and diarrhea stomach pain or cramps, anorexia; Symptoms of nerve system include headache and swirl; Abnormal sensation, numb limbs and tense tendons, ataxia, and multiple neuritis occasionally happen; Over high dose can cause convulsion. Few cases have the symptoms such as urticaria, moisst, pruritus, cystitis, dysuresia, change in taste sensation and decreased white cell. But the abovementioned symptoms are all reversible and recover after the administration.
Contraindication
Forbid to use the medicine for the patients with the diseases in central nervous system and flood.
Indication for women in pregnant and suckle
Forbid to use this medicine for women in pregnant and suckle.
Substance interactions
 
Overdose High dose may cause convulsion.
Storage: Instructions Light-resistant and store in well-closed containers.
Packaging: Poloypropylene bottle; Non-PVC Bag; Glass bottle
Metronidazole Injection 100ml:0.5g
100ml:0.5g (PP)
40
80
440×300×150
470×370×250
1425
648
10.7
8
 
BASIC INJECTIONS -Large Volume
Product name Strength
Sodium Chloride Injection 0.9%,100/250/500/1000ml
Sodium Lactate Ringer's Injection 500ml/1000ml
Ringer's Injection
(Compound Sodium Chloride Injection)
250ml/500ml/1000ml
Glucose(Dextrose) Injection 5%,50/100/200/250/500/1000ml
10%,50/100/200/250/500/1000ml
Glucose and Sodium Chloride Injection (5+0.9)%, 100/250/500/1000ml
(5+0.45)%, 100/250/500/1000ml
Glucose and Sodium Chloride Potassium Chloride Injection 250ml
Xylitol Injection 5%,250/500ml
Sterile Water for Injection 100/250/500/1000ml

Service we can provide:
1. Mixed container, we can mix different items in one container.
2. Quality control, before shipment, free sample for test. After shipment, keep sample for 3 years
3. Prompt shipment with professional documents
4. Packing as your request, with photo before shipment.

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To get more information, just feel free to contact with us. Thanks.
Mr. Liu
Qingdao Fraken International Trading Co., Ltd
Address: RM1005 post mansion yan'an three road, Qingdao, China
Web: http://fraken.en.made-in-china.com/

GMP Certified 0.5% Metronidazole Infusion &amp; Metronidazole Injection
GMP Certified 0.5% Metronidazole Infusion &amp; Metronidazole Injection
GMP Certified 0.5% Metronidazole Infusion &amp; Metronidazole Injection
GMP Certified 0.5% Metronidazole Infusion &amp; Metronidazole Injection
GMP Certified 0.5% Metronidazole Infusion &amp; Metronidazole Injection

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Rating: 5.0/5
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ISO 9001, ISO 14000, ISO 20000, GMP, HACCP
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