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Product's Key Features
Urokinase 5000 IU
Contains Urokinase IP at a strength of 5000 IU per vial.
Lyophilized formulation
Supplied as a lyophilized injectable preparation requiring preparation according to the approved product instructions.
IV administration
The package specifically states "For IV Use Only."
Single-dose vial
The pack states that the vial is a single-dose container and unused portion should be discarded.
Temperature-sensitive storage
Store at 2°C–8°C and protect from light, as stated on the product packaging.
Prescription medicine
The package carries the Schedule H prescription drug caution.
Precautions & Warnings
Prescription medicine — use only under medical supervision.
- Not intended for self-administration.
- For IV use only.
- Dosage and administration must be determined by the treating physician.
- Follow the package insert for reconstitution and administration instructions.
- Store at 2°C–8°C and protect from light.
- Do not use the solution if foreign particles are visible after reconstitution, as stated on the package.
- The vial is intended for single-dose use; discard any unused portion.
- Keep out of reach of children.
- Patients should inform their healthcare professional about relevant medical conditions, medications and bleeding risks before treatment.
Urokinase can cause serious bleeding and other adverse effects; the National Formulary lists bleeding, hypotension, arrhythmias and allergic reactions among possible adverse effects
Clinical Role & Safety Information
Clinical Role
Urokinase is a fibrinolytic/thrombolytic medicine used in clinical settings to help dissolve blood clots in specific medical conditions. Its use, dosage and administration must be determined by the treating physician. The National Formulary of India lists clinical uses including conditions such as deep-vein thrombosis, pulmonary embolism and certain arterial or peripheral vascular thromboses.
Safety Information
Urokinase therapy can carry significant bleeding and other medical risks. Treatment should be initiated and monitored by an appropriately qualified healthcare professional after assessment of the patient's condition, bleeding risk, contraindications and concomitant medicines. Refer to the approved prescribing information/package insert before use.
Why Customers Choose HealthOra
We combine quality, affordability, and reliable service to create a better healthcare purchasing experience.
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FAQ - Frequently Asked Questions
Is a prescription required for RECATH Urokinase 5000 IU Injection?
Is a prescription required for RECATH Urokinase 5000 IU Injection?
Yes. RECATH Urokinase 5000 IU Injection is a Schedule H prescription medicine. It should be supplied only against a valid prescription from a Registered Medical Practitioner and used under appropriate medical supervision.
How should RECATH Urokinase 5000 IU Injection be stored?
How should RECATH Urokinase 5000 IU Injection be stored?
The product packaging states that it should be stored at 2°C–8°C and protected from light. Please follow the storage conditions printed on the product packaging and package insert.
How is RECATH Urokinase 5000 IU Injection administered?
How is RECATH Urokinase 5000 IU Injection administered?
The product is a lyophilized injection marked "For IV Use Only." Reconstitution, dosage and administration should be carried out strictly according to the approved product instructions and the treating physician's direction.
How quickly will my order be delivered?
How quickly will my order be delivered?
Orders are generally dispatched within 24 hours after order confirmation and required prescription verification. Delivery typically takes 2–5 business days, depending on the destination, courier service, weekends, public holidays, festivals and other logistical circumstances.
What should I do if my medicine arrives damaged?
What should I do if my medicine arrives damaged?
Please check the package promptly after delivery. If you receive a damaged, incorrect or visibly compromised product, contact Healthora Plus Support as soon as possible with photographs of the package and product so the issue can be reviewed.