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3.75 MG Leuprolide Acetate For Injection

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3.75 MG Leuprolide Acetate For Injection

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MOQ : 10 Units

3.75 MG Leuprolide Acetate For Injection Specification

Salt Composition
Leuprolide Acetate 3.75 mg per vial

Indication
Used in the management of prostate cancer, endometriosis, uterine fibroids, and central precocious puberty

Dosage Form
Lyophilized powder for injection

Enzyme Types
Not applicable (Synthetic peptide analog)

Feature
GMP certified, high purity, controlled release

Ingredients
Leuprolide Acetate, suitable excipients

Application
Parenteral (subcutaneous or intramuscular) administration

Physical Color/Texture
White to off-white lyophilized powder

Fermentation Smell
Odorless

Storage Instructions
Dry place

Shelf Life
24 months from the date of manufacture

Instructions for Use
Use immediately after reconstitution; discard unused portion

Prescription Status
Prescription only medicine

Reconstitution Details
Reconstitute with provided diluent before administration

Pack Size
Single-dose vial with one vial of solvent for reconstitution

Administration Route
Subcutaneous or intramuscular injection

Mode of Action
GnRH agonist - suppresses gonadotropin secretion

Contraindications
Hypersensitivity to leuprolide acetate or any excipients

USP/Quality Standard
Meets pharmacopoeial quality standards

3.75 MG Leuprolide Acetate For Injection Trade Information

Minimum Order Quantity
10 Units

Payment Terms
Cash Advance (CA)

Supply Ability
5000 Units Per Month

Delivery Time
5-7 Days

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

About 3.75 MG Leuprolide Acetate For Injection

Capitalise on the perfect solution for hormone-related conditions with 3.75 MG Leuprolide Acetate For Injection. This unbeatable single-dose vial comes complete with a vial of solvent for advance purchase, allowing you to buy online with confidence. As a kingly, GMP-certified synthetic peptide analog, it meets strict pharmacopoeial quality standards and ensures high purity as well as controlled release. Ideal for prostate cancer, endometriosis, uterine fibroids, and central precocious puberty. Administer subcutaneously or intramuscularly after reconstitution. Use as directed by your healthcare professional. Exporter, supplier, trader from India.

Primary Competitive Advantages & Usage Benefits

3.75 MG Leuprolide Acetate For Injection offers reliability through GMP certification, high purity, and a controlled release mechanism, setting it apart from competitors. This prescription-only lyophilized powder is easy to reconstitute and suitable for subcutaneous or intramuscular application. Perfect for managing prostate cancer, endometriosis, uterine fibroids, and central precocious puberty, its single-dose packaging ensures precise dosing and minimal wastage. Choose advance purchase to secure availability and benefit from its proven efficacy in hormone regulation.

Supply Ability, Domestic Market & Transport Support

With robust supply ability and a focus on timely arrival, 3.75 MG Leuprolide Acetate For Injection is available for immediate dispatch across India's main domestic markets. Packaging is meticulously handled to preserve product integrity during transit. We utilize comprehensive transport services through our trusted FOB ports in India, ensuring your advance purchase reaches you quickly and securely. Choose our kingly injectable solution for seamless and reliable supply every time.

FAQ's of 3.75 MG Leuprolide Acetate For Injection:

Q: How should 3.75 MG Leuprolide Acetate For Injection be administered?

A: This medication is administered either subcutaneously or intramuscularly. Reconstitute the lyophilized powder with the provided vial of solvent immediately before use, and discard any unused portion.

Q: What are the main indications for using Leuprolide Acetate For Injection?

A: Leuprolide Acetate is used for the management of prostate cancer, endometriosis, uterine fibroids, and central precocious puberty as directed by a healthcare professional.

Q: When should the injection be used after reconstitution?

A: The injection should be used immediately after reconstituting the powder with the supplied solvent; any remaining mixture must be discarded.

Q: Where should the product be stored for optimal quality?

A: Store the product in a dry place as directed in the storage instructions and keep it away from sources of moisture and excessive heat.

Q: What is the process for reconstituting this injection?

A: To reconstitute, add the provided vial of solvent to the lyophilized powder and mix gently until fully dissolved. Administer the solution right after preparing it.

Q: What are the competitive advantages of purchasing this product online?

A: Buying online ensures advance purchase and consistent availability, along with the guarantee of receiving a GMP-certified, high-purity product that meets pharmacopoeial quality standards.

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