Seftakar & Seftranaz

Seftakar & Seftranaz

Product Details:

  • Salt Composition Ceftriaxone 1000 mg + Tazobactam 125 mg
  • Indication Treatment of susceptible bacterial infections
  • Dosage Form Injection
  • Pacakaging (Quantity Per Box) 1 Vial + 1 Ampoule of Sterile Water for Injection
  • Origin of Medicine India
  • Drug Type Prescription
  • Ingredients Ceftriaxone and Tazobactam
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Seftakar & Seftranaz Price And Quantity

Seftakar & Seftranaz Product Specifications

  • Powder for Injection
  • Bacterial Infections
  • Treatment of susceptible bacterial infections
  • Adults and Children
  • 1 Vial + 1 Ampoule of Sterile Water for Injection
  • Store in a cool and dry place below 25C, protect from light
  • 1 vial per box
  • Injection
  • Ceftriaxone and Tazobactam
  • Prescription
  • India
  • As directed by physician
  • To be administered by a registered medical practitioner
  • Antibiotic
  • Ceftriaxone 1000 mg + Tazobactam 125 mg

Seftakar & Seftranaz Trade Information

  • Telegraphic Transfer (T/T), Cheque
  • Depends On requirement Week
  • Yes
  • Contact us for information regarding our sample policy
  • Customized Packaging
  • Australia, North America, Eastern Europe, Middle East, Western Europe, Africa, Central America, South America, Asia

Product Description

ANTIBIOTIC/ ANTIFUNGAL /
ANTIMALARIAL / ANTI - INFECTIVES




Azithromycin 250mg

TABLET
Azithromycin 500mg

TABLET
Ofloxacin 200mg

TABLET
Ofloxacin 400mg

TABLET
Ofloxacin 200mg + Ornidazole 500mg

TABLET
Cefpodoxime 50mg

TABLET
Cefpodoxime 100mg (Dispersible Tablet)

TABLET
Cefpodoxime 200mg

TABLET
Cefpodoxime 200mg + Clavulanic Acid 125mg

TABLET
Cefpodoxime 200mg + Azithromycin 250mg

TABLET
Cefpodoxime 200mg + Dicloxacillin 500mg (ER)

TABLET
Cefpodoxime 200mg + Levofloxacin 250mg

TABLET
Cefixime Trihydrate 50mg

TABLET
Cefixime Trihydrate 100mg (Dispersible Tablet)

TABLET
Cefixime Trihydrate 200mg

TABLET
Cefixime 50mg + Clavulanic Acid 31.25mg

TABLET
Cefixime 100mg + Clavulanic Acid 62.5mg

TABLET
Cefixime 200mg + Clavulanic Acid 125mg

TABLET
Cefixime Trihydrate 200mg + Dicloxacillin 500mg (Ext. Rel.)

TABLET
Cefixime 200mg + Ofloxacin 200mg

TABLET
Cefixime 200mg + Ornidazole 500mg

TABLET
Cefixime 200mg + Azithromycin 250mg

TABLET
Amoxycillin 200mg + Clavulanic Acid 28.5mg

TABLET
Amoxycillin 250mg + Clavulanic Acid 125mg

TABLET
Amoxycillin 500mg + Clavulanic Acid 125mg

TABLET
Amoxycillin 875mg + Clavulanic Acid 125mg

TABLET
Cefuroxime 250mg

TABLET
Cefuroxime 500mg

TABLET
Cefuroxime 250mg + Clavulanic Acid 125mg

TABLET
Cefuroxime 500mg + Clavulanic Acid 125mg

TABLET
Linezolid 600mg

TABLET
Levofloxacin 250mg

TABLET
Levofloxacin 500mg

TABLET
Levofloxacin 750mg

TABLET
Ciprofloxacin 500 mg

TABLET
Amoxycillin 250mg + Dicloxacillin 250mg

CAPSULE
Cefpodoxime 50mg / 5ml

DRY SYRUP
Cefpodoxime 50mg + Clavulanic Acid 31.25mg/5ml

DRY SYRUP
Cefixime 50mg/5ml

DRY SYRUP
Cefixime 50mg + Clavulanic Acid 31.25mg/5ml

DRY SYRUP
Amoxycillin 200mg + Clavulanic Acid 28.5mg/5ml

DRY SYRUP
Cefpodoxime 100mg/5ml

DRY SYRUP
Azithromycin Suspension 100mg

SUSPENSION

                               






Broad-Spectrum Antibacterial Protection

Seftakar & Seftranaz utilize a robust combination of Ceftriaxone and Tazobactam, targeting a wide range of bacterial pathogens. This combination enhances antibiotic effectiveness against both Gram-positive and Gram-negative bacteria by preventing bacterial resistance, making it a reliable choice for complex infections.


Convenient Powder for Injection Formulation

Each vial is packaged with a matching ampoule of sterile water, designed for on-the-spot reconstitution. This ensures high potency and stability while allowing administration via intravenous or intramuscular injection, facilitated by medical professionals for precision and safety during therapy.


Stringent Storage and Shelf Life Guidelines

Seftakar & Seftranaz are formulated to maintain stability for up to 24 months when stored correctly below 25C and protected from light. Careful adherence to storage requirements preserves the drugs effectiveness, offering peace of mind to healthcare providers and patients alike.

FAQs of Seftakar & Seftranaz:


Q: How should Seftakar & Seftranaz be administered?

A: Seftakar & Seftranaz are intended for intravenous or intramuscular injection. The powder must be reconstituted with the supplied sterile water by a registered medical practitioner before administration to ensure proper dosage and effectiveness.

Q: What is the recommended storage condition for this medication?

A: The vials should be stored in a cool, dry place below 25C and protected from direct light. Adhering to these conditions helps maintain the medications stability and potency throughout its 24-month shelf life.

Q: Who can use Seftakar & Seftranaz, and for what kind of infections are they prescribed?

A: These antibiotics are suitable for both adults and children and are indicated for the treatment of bacterial infections susceptible to Ceftriaxone and Tazobactam, as determined by a physician.

Q: When should the product be reconstituted, and what should be used for this process?

A: The injection should be reconstituted immediately before use, using only the sterile water ampoule provided in the packaging. This ensures the medication remains stable and effective until administration.

Q: What are the primary ingredients in Seftakar & Seftranaz, and how do they work?

A: Each vial contains Ceftriaxone (1000 mg) and Tazobactam (125 mg). Ceftriaxone kills bacteria by disrupting their cell wall synthesis, while Tazobactam inhibits beta-lactamase enzymes that some bacteria use to resist antibiotics.

Q: Are there any contraindications for using this product?

A: Seftakar & Seftranaz should not be used in patients with known hypersensitivity to cephalosporins, beta-lactam antibiotics, or any ingredients in the formulation. Inform your doctor of any allergies before starting treatment.

Q: Can the medicine be used without a prescription, and who should administer it?

A: No, Seftakar & Seftranaz are prescription-only medications (Rx Only) and must be used under medical supervision. Administration should be performed by a registered medical practitioner to ensure correct reconstitution and dosage.

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