Chengdu Xinheng Pharmaceutical Co.,Ltd

Business Type:Manufacturer

Main Products: Penicillin G Procaine and Dihydrostreptomycin Sulfate InjectionOxytetracycline InjectionAmoxicillin InjectionCeftiofur Hydrochloride Ketoprofen InjectionIvermectin InjectionFlorfenicol InjectionAmoxicillin +Gentamycin InjectionAlbendazole SuspensionToltrazuril Oral Solution

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Ceftiofur Hydrochloride Ketoprofen Injection

Agricultural Animal-breeding

EXW Price:US$ 4.20 / Piece(s)

MOQ:5000 Piece(s)

Payment Method : T/T 

Keywords:antibiotic injection 

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Product Category: Agricultural > Animal-breeding Trademark: xinheng
Product Package: colorless glass bottle Specifications: 100ml, 5%Ceftiofur Hydrochloride and 15%Ketoprofen Injection
Place of Origin: Chengdu, Sichuan Port: Yanshan Deep-water Port

Characteristics: This product is suspension of fine particles, fine particle sinking after static position, shake to become a uniform milky white suspension.

Identification: (1) In a chromatogram recorded under the determination of content, the retention time of the major peak of the test solution corresponds to that of the reference solution of Ceftiofur Hydrochloride Ketoprofen Injection.

(2) Take the product 0.5mladding ethanol 1ml to dissolve, add two 4-dinitrophenylhydrazine TS 1ml, shake well, heating to boiling, then cooling, then produce a kind of orange-red precipitate.

Test (Sterility): 10 bottles of this product are taken as samples, take 10ml per bottle (shake well before use), after mixing, take 25ml, add aseptic 1% Twain -80 and 0.1% peptone solution 250ml, fully shake to disperse, then add the penicillin enzyme solution (about 14400IU penicillin enzyme per 1mg this product), fully shake for 30 minutes, take mixing liquid 10ml, add separately to fluid thioglycollate medium and Modified Martin Broth, 14 days of rocking bed culture under the corresponding conditions, inoculating culture medium on the slope culture medium, 2 days of bacterial culture and 3 days of fungal , in accordance with the rules, the results should be in accordance with the regulations culture.

Others: Should comply with the relevant provisions of the injections.

Assay of content

Ceftiofur Hydrochloride: Assay according to high performance liquid chromatography.

Test of chromatographic conditions and system applicability: Use octadecylsilane bonded silica gel as filler; the detection wavelength is 254nm. The degree of separation between the ceftiofur peak and the peak of the internal standard should be in accordance with the requirements.

Mobile phase preparation: Take 3.85g ammonium acetate, add four butyl hydroxide ammonium hydroxide solution(10100)54ml, Add deionized water to 700ml, adjust pH value to 6.6 ~ 6.8 with glacial acetic acid, then add methanol 200ml and tetrahydrofuran 110ml, shake well.

Preparation of internal standard solution: Take the appropriate quantity of ethylparaben, add ammonium acetate solution0.05molL, to get a solution containing 50ug in each 1ml, shake well until dissolved.

Assay method: Take this product 5ml, precision weighing, put in a 25ml graduated flask, dissolving and diluting to scale with two methyl formamide - n-butanol (1:1), shake well, use precision instruments to weigh and take 1ml, add acetonitrile water (1:1) 10ml, N-hexane 5ml, oscillate and shake for 2 minutes, centrifugal, measuring and taking the lower layer solution 1ml with a precision instrument, then add internal standard solution 10ml, shake well, take 20ul into HPLC, recording chromatogram; take 25mg standard product of Ceftiofur Hydrochloride, precision weighing, put in a 25ml graduated flask, dissolving and diluting to scale with two methyl formamide - n-butanol (1:1) 2.5ml and acetonitrile water (1:1) , shake well, use precision instruments to weigh and take 1ml, then add internal standard solution 10ml, shake well, take 20ul into HPLC, recording chromatogram, calculation of peak area by internal standard method, and then take this product, measure relative density at the same time, convert the quantity of the sample into milliliter, then calculate.    

Ketoprofen: Assay according to high performance liquid chromatography.

Test of chromatographic conditions and system applicabilityUse octadecylsilane bonded silica gel as filler, Use phosphate buffer liquid(take Potassium dihydrogen phosphate 6.8g, add water, dissolve and dilute to 100ml, use phosphoric acid to adjust the pH to 3.5 + 0.1) – acetonitrile - water 24355as mobile phase; the detection wavelength is 255nm. The number of theoretical plates is calculated according to the peak of ketoprofenshould not less than 2000.

Assay method: Weigh with a precision instrument and take the appropriate amount of the product, after the quantitative dilution of the mobile phase, prepare the solution per 1ml contains about 0.1mg of ketoprofen, weigh with precision instrument and take 10ul put into HPLC, recording chromatogram; then take the standard product of ketoprofen, assay with the same method, calculate the peak area by external standard method. Then take this product, measure relative density at the same time, convert the quantity of the sample into milliliter, then calculate. 

Indication: Same with Ceftiofur Hydrochloride Ketoprofen.

Dosage and Administration:  

Intramuscular injection

Cattle: Bacterial respiratory infections : 1 ml per 50 kg body weight for 3 - 5 days.

Acute interdigital necrobacillosis (panaritium, foot rot) : 1 ml per 50 kg body weight for 3 days.

Acute metritis (0 - 10 days post partum) : 1 ml per 50 kg body weight for 5 days.

Swine: Bacterial respiratory infections : 1 ml per 50 kg body weight for 3 days.


Contact Name: Mr chong dai Contact Email: cd****g@vip.sina.com
Contact Job Title: Business Man Contact Mob: 136***572
Contact Tel: Contact Fax:
Address: 新都区工业开发东区白云路439号 Website: www.cdxinheng.com

Chengdu Xinheng Pharmaceutical Co.,Ltd, lies in No. 439, Baiyun road, Xindu industrial zone, Chengdu, Sichuan Province, China, Founded in 1996, as the leading manufacturer of veterinary medicine products in China, has more than 120 employees, the total area of the factory is 32000 square meters, the facilities are designed and constructed strictly according to GMP requirements. All production lines, in March 2007, Xinheng Pharma passed the GMP inspection and GMP authorized by Chinese Ministry of Agriculture.

In December 2019, Xinheng passed the GMP re-inspection of Ministry of Agriculture, certificated No. (2020) 22005 ; the certificated scope are Powder/Pulvis/Premix, Terminally Sterilized Small Volume Injection/ Terminally Sterilized Large Volume Non-Intravenous Injection, Intramammary Infusion.

After ten years development, now Chengdu Xinheng pharma has 6 workshops and 11 production lines as below:

1Sterile powder for injection, 

2Final sterile injection large/small volume,

3Oral solution,

4Premix/Powder/Chinese medicine pulvis,

5Non-final sterile injection large/small volume,

6Non-final sterile Intramammary/Uterine Infusion.

We have a strong R&D team, and QC laboratory to guarantee the high quality products, particularly For the quality of suspension injection produced by our company is a first-class level top quality in the industry. We execute strictly veterinary standard according to the Ministry of Agriculture and we also can supply products fully comply with EP and USP standard according to the customer requirements. The research and development department is seeking for high quality and innovated products, offering more effective and safer products for users and customers.

Since 2008, products of Xinheng Pharma exported to Europe, Asia, such as Holland, Germany, Korea, Mongolia etc., all the samples passed the test of EU BACTIM.


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