Tranadol Injection

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Tranadol Injection Specification

Origin of Medicine
Allopathic

Salt Composition
Tramadol Hydrochloride

Indication
Moderate to severe pain

Dosage Form
Injection

Pacakaging (Quantity Per Box)
10 ampoules per box

Drug Type
Generic

Ingredients
Tramadol Hydrochloride

Physical Form
Liquid

Function
Pain Relief

Recommended For
Adults

Dosage
As directed by physician

Dosage Guidelines
Intravenous or intramuscular injection

Suitable For
Suitable for adults

Quantity
Multiple packaging options

Storage Instructions
Store below 25C, protect from light

Color
Clear or slightly yellowish solution

Pack Size
2ml per ampoule

Container Type
Glass ampoule

Application
Hospital, clinical and medical use

Strength
50 mg/ml

Route of Administration
Intravenous, Intramuscular

Expiry
36 months from date of manufacture

Tranadol 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

Main Export Market(s)
Middle East, Asia, South America, Western Europe, Africa, Australia, Central America, North America, Eastern Europe

About Tranadol Injection

Form	Injection
Usage/Application	Hospital
Prescription/Non prescription	Non prescription
Purity	98 %
Shelf Life	24 Month
Minimum Order Quantity	100

An injection is a shot, or a dose of medicine given by way of a syringe and a needle. When you get jabbed in the arm with a tetanus vaccine, that's an injection. The medical kind of injection forces a small amount of a drug under the skin or directly into a muscle.

Advanced Pain Relief Solution

Tranadol Injection is specifically designed to deliver fast and effective relief from moderate to severe pain in adults. Its high-quality formulation ensures safe and reliable pain management in clinical, hospital, or medical settings. Packaged in sturdy glass ampoules, Tranadol maintains its efficacy and sterility until administration, making it a trusted choice for healthcare professionals.

Versatile Administration Options

Administered intravenously or intramuscularly, Tranadol Injection offers flexibility to healthcare providers, adapting to the patient's needs and the specifics of the medical situation. Tramadol Hydrochloride acts promptly once administered, providing consistent and sustained pain relief for various acute or chronic conditions.

Safe Storage & Lasting Potency

To preserve Tranadol Injection's optimal effectiveness, store the product below 25C and protect it from light. Each ampoule contains a clear or slightly yellow solution, ensuring easy inspection before use. The product retains its potency for up to 36 months from the manufacturing date, delivering consistent results throughout its shelf life.

FAQ's of Tranadol Injection:

Q: How is Tranadol Injection administered to patients?

A: Tranadol Injection is administered either intravenously or intramuscularly by a qualified healthcare professional, based on the physician's guidance and the patient's specific pain management requirements.

Q: What are the main indications for using Tranadol Injection?

A: Tranadol Injection is recommended for the relief of moderate to severe pain in adults, particularly in hospital, clinical, and various medical settings.

Q: When should Tranadol Injection be used?

A: Tranadol Injection should be used when prompt and effective management of moderate to severe pain is necessary, always under the supervision and dosage instructions of a healthcare provider.

Q: Where should Tranadol Injection be stored to maintain its quality?

A: Store Tranadol Injection below 25C in a location protected from light to preserve its efficacy and potency throughout its shelf life.

Q: What is the benefit of choosing Tranadol Injection for pain relief?

A: Tranadol Injection provides rapid and sustained pain relief, making it suitable for acute or chronic pain scenarios in adult patients; its formulation in glass ampoules ensures sterility and accurate dosing.

Q: What is the process for preparing and administering Tranadol Injection?

A: A healthcare professional will inspect the ampoule (clear or slightly yellowish solution), withdraw the prescribed dose (typically 50 mg/ml), and administer it via the chosen route-either intravenous or intramuscular injection.

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