Facilitation of tracheal intubation, maintenance of skeletal muscle relaxation during surgery or mechanical ventilation
Dosage Form
Injection
Origin of Medicine
Synthetic
Pacakaging (Quantity Per Box)
Typically 10 vials per box
Salt Composition
Atracurium Besylate 100mg
Drug Type
Allopathic
Ingredients
Atracurium Besylate
Physical Form
Liquid
Function
Non-depolarizing neuromuscular blocking agent
Recommended For
Anesthesia adjunct, skeletal muscle relaxation
Dosage
100 mg per injection
Dosage Guidelines
Administer intravenously; use as directed by physician
Suitable For
Adults & pediatric patients (under medical supervision)
Quantity
As per packaging vial; standard is 2.5 ml per vial
Storage Instructions
Store between 2C to 8C, protect from light
Shelf Life
24 months from manufacture
Appearance
Clear, colorless to pale yellow solution
Brand Name
Artacil
Regulatory Status
Banned for use in some countries; check local approval
Marketed By
As per packaging label
Compatibility
Compatible with common IV fluids
Prescription/Non-Prescription
Prescription Only
Contraindications
Hypersensitivity to Atracurium or components
Precautions
For hospital/clinical use; administer under supervision of trained personnel
Route of Administration
Intravenous (IV) use only
Atracurium Besylate Liquid 100mg Artacil Injection Trade Information
Supply Ability
1000 Per Day
Delivery Time
7 Days
Sample Available
No
Sample Policy
Contact us for information regarding our sample policy
About Atracurium Besylate Liquid 100mg Artacil Injection
Packaging Type
Vial
Brand
Artacil
Usage/Application
Clinical
Composition
Atracurium Besylate
Injectable Form
Liquid
Packaging Size
10ml
Strength
100mg
Prescription/ Non Prescription
Prescription
Country of Origin
Made in India
Artacil 100 Injection belongs to a group of medicines called muscle relaxants. It is used along with general anesthesia or sedatives to provide skeletal muscle relaxation during surgical procedures. It is also used to facilitate emergency airway management in patients in intensive care.
Effective Adjunct for Anesthesia
Artacil is engineered to enhance anesthesia outcomes, making tracheal intubation and surgical muscle relaxation safer and more predictable. By working as a neuromuscular blocker, it assists healthcare teams in maintaining optimal muscle control during critical procedures.
Strict Safety and Compatibility Guidelines
Artacil must be administered intravenously by trained professionals to ensure patient safety. It is compatible with standard IV fluids and designed for use in controlled hospital or clinical environments, minimizing risks and supporting effective surgical care.
FAQ's of Atracurium Besylate Liquid 100mg Artacil Injection:
Q: How should Artacil (Atracurium Besylate Injection) be administered?
A: Artacil is given intravenously by a healthcare professional, typically in hospital or clinical settings. It should be administered according to a physician's guidance to ensure safe and effective muscle relaxation.
Q: What is the recommended storage condition for Artacil vials?
A: Artacil should be stored between 2C and 8C and protected from light. Proper storage maintains the stability and effectiveness of the medication over its 24-month shelf life.
Q: When is Artacil typically used during medical procedures?
A: Artacil is employed during anesthesia for tracheal intubation, and to maintain skeletal muscle relaxation throughout surgical operations or mechanical ventilation.
Q: Where should Artacil be administered to ensure patient safety?
A: Artacil is intended exclusively for use in hospitals or clinical settings, under the supervision of trained medical personnel, due to its potent effects and necessity for precise dosing.
Q: What is the primary benefit of using Artacil in surgeries?
A: Artacil provides controlled muscle relaxation, improving surgical conditions and facilitating airway management, which contributes to safer and more efficient procedures.
Q: Who is eligible for Artacil administration?
A: Artacil may be given to adults and pediatric patients needing anesthesia, but only when closely supervised by medical experts, and after ruling out hypersensitivity to its ingredients.
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