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ANHUI BBCA PHARMACEUTICAL CO.,LTD
ANHUI BBCA PHARMACEUTICAL CO.,LTD
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Powder for Injection Pharmaceutical Grade Cefotaxime Sodium for Injection

Product Details

Certification: GMP

Model Number: BBCA18022713

Payment & Shipping Terms

Price: Negotiated

Packaging Details: 10VialsX100Boxes/Carton

Delivery Time: 25 DAYS AFTER PAYMENT

Payment Terms: L/C, T/T, , MoneyGram, L/C, T/T, , MoneyGram

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Specifications
Highlight:

pantoprazole sodium

,

pantoprazole sodium sesquihydrate

Place Of Origin:
China (Mainland)
Brand Name:
BBCA
Other Names:
Powder For Injection Pharmaceutical Grade Cefotaxime Sodium For Injection
Grade:
Medicine Grade
Dosage Form:
Injection
Place Of Origin:
China (Mainland)
Brand Name:
BBCA
Other Names:
Powder For Injection Pharmaceutical Grade Cefotaxime Sodium For Injection
Grade:
Medicine Grade
Dosage Form:
Injection
Description
Powder for Injection Pharmaceutical Grade Cefotaxime Sodium for Injection

Specifications

1. Product Name: Powder for Injection Pharmaceutical Grade Cefotaxime Sodium for Injection

 

2. Component: This article main ingredients for cefotaxime sodium.

 

3. Appearance: This product is a white to yellowish white crystalline powder.

 

4. Indications:  Suitable for pneumonia caused by sensitive bacteria and other lower respiratory tract infection, urinary tract infections, meningitis, septicemia, abdominal cavity infection, pelvic infection, skin soft tissue infection, reproductive tract infections, bone and joint infections, etc.Cefotaxime can be used as a selection of infantile meningitis drugs.

 

5. Specifications: 0.5g: 1.0g

 

6. Usage and Dosage:  

 
Adult day 2 ~ 6 g, 2 ~ 3 times intravenous injection or intravenous drip;Serious infections every 2 ~ 3 g, 6 ~ 8 hours a day the highest dose not more than 12 g.Treatment of uncomplicated pneumococcal pneumonia or acute urinary tract infection, 1 g every 12 hours.
Newborn babies less than or equal to 7 day age 50 mgPowder for Injection Pharmaceutical Grade Cefotaxime Sodium for Injection 0 every 12 hours, and born more than 7, 50 mgPowder for Injection Pharmaceutical Grade Cefotaxime Sodium for Injection 0 every 8 hours.Meningitis patients treated dose may be increased to 75 mgPowder for Injection Pharmaceutical Grade Cefotaxime Sodium for Injection 0 every 6 hours, to intravenous drug delivery.
Patients with severe renal impairment when the application of this product must be appropriate reduction.Serum creatinine values of more than 424 mu mol/L (4.8 mg), or less than 20 ml/creatinine clearance, the product maintenance quantity should be halved;More than 751 mu of serum creatinine mol/L (8.5 mg), maintain the quantity for the normal amount of a quarter.Need hemodialysis is 0.5 ~ 2 g a day.But after dialysis dose should add in 1 time.

 

7. Contraindications:  Allergic to cephalosporin and has a history of penicillin anaphylactic shock or immediate reaction to disable this product.

 

8. Storage: Protect from light, airtight preservation,and stored within temperature of 20℃.

 

9. Package: 10 Vials/Box; 100 Boxes/Carton

 

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