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Aztreonam For Injection USP
Aztreonam For Injection USP

Aztreonam For Injection USP

Price 1200 INR/ Unit

MOQ : 1 Unit

Aztreonam For Injection USP Specification

  • Pacakaging (Quantity Per Box)
  • 1 gm
  • Brand Name
  • Zeonam
  • Salt Composition
  • Aztreonam
  • Packaging Type
  • Box
  • Indication
  • Bacterial infections including respiratory tract
  • Dosage Form
  • Injection
  • Drug Type
  • Prescription
  • Function
  • Antibacterial
  • Storage
  • Below 25C
  • Route of Administration
  • IV/IM
  • Single Dose Vial
  • Yes
  • Colour
  • White powder
  • Reconstitution
  • Required before use
  • Solubility
  • Water-soluble
  • Sterility
  • Sterile
  • USP Grade
  • Complies
  • Prescription Required
  • Yes
 

Aztreonam For Injection USP Trade Information

  • Minimum Order Quantity
  • 1 Unit
  • Payment Terms
  • Cash in Advance (CID)
  • Supply Ability
  • 1000 Units Per Month
  • Delivery Time
  • 7 Days
  • Main Domestic Market
  • All India
 

About Aztreonam For Injection USP



Spotlight your healthcare inventory with Zeonam - Aztreonam For Injection USP, a top-rated, in-demand solution for effectively combating bacterial infections. This eminent, classic antibiotic comes as a potent, sterile white powder designed for IV or IM administration. Packaged in single-dose vials, Zeonam is water-soluble and must be reconstituted before use. Adhering to USP grade standards, it requires refrigeration below 25C to ensure maximum efficacy. Its trusted antibacterial function makes it a prescription-only choice for healthcare professionals treating various respiratory and other bacterial infections across India.

Area of Application and Use Type

Aztreonam For Injection USP is widely utilized in both hospitals and clinics for combating severe bacterial infections, particularly those affecting the respiratory tract. Designed for use on human tissue via intravenous or intramuscular routes, this antibacterial agent effectively treats infections at the source. The use type is strictly for prescription administration, ensuring safety and efficacy under professional supervision, making it an indispensable option for medical practitioners managing critical care situations.


Packaging, Domestic Market, and Secure Shipment

Serving the export market across India, Aztreonam For Injection USP is available in a robust, single-dose 1 gm vial, securely packed in boxes to ensure product purity. With a focus on secure shipping and meticulous packaging details, every shipment is dispatched to guarantee sterility and safety through transit. Delivery times are dependable, catering to the needs of domestic hospitals and pharmacies, meeting urgent demand efficiently and reliably throughout the nation.


FAQ's of Aztreonam For Injection USP:


Q: How should Aztreonam For Injection USP be prepared before administration?

A: Aztreonam For Injection USP must be reconstituted with an appropriate sterile solution before intravenous or intramuscular injection, as per the prescribing information.

Q: What are the main indications for using Zeonam Aztreonam For Injection USP?

A: Zeonam is primarily indicated for the treatment of bacterial infections, including infections of the respiratory tract and other susceptible pathogens.

Q: When is it appropriate to administer Aztreonam For Injection USP via IV or IM route?

A: The injection is administered intravenously or intramuscularly depending on the severity and type of infection, as assessed by a qualified healthcare provider.

Q: Where should Aztreonam For Injection USP be stored for optimal potency?

A: This medication should be stored below 25C to maintain its sterility and effectiveness until it is ready for use.

Q: What processes are involved in exporting Aztreonam For Injection USP from India?

A: A secure shipping and packaging protocol is followed, ensuring the product reaches buyers in pristine, sterile condition, complying with export market standards.

Q: What are the benefits of using a single-dose vial of Aztreonam For Injection USP?

A: Using a single-dose vial minimizes contamination risk, ensures precise dosage, and upholds the sterility of each administration for patient safety.

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