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LUPRODEX 3.75 MG INJ

Name: LUPRODEX 3.75 MG INJ
Brand: FOURWAY PHARMA LLP
Price: 2980 INR
Availability: InStock

Price 2980 INR/ Unit

Get a Price/Quote

MOQ : 100 Units

LUPRODEX 3.75 MG INJ Specification

Dosage Form
Injection

Pacakaging (Quantity Per Box)
1 Vial, 2 ml

Packaging Type
Vial

Brand Name
Luprodex

Salt Composition
Leuprolide Acetate

Origin of Medicine
India

Life Span
24 months

Indication
Prostate Cancer

Drug Type
Depot

Ingredients
Leuprolide Acetate

Physical Form
Injection

Function
Hormonal Therapy

Recommended For
Prostate Cancer

Dosage
3.75 mg

Dosage Guidelines
As directed by physician

Suitable For
Adults

Quantity
1 x 2

Storage Instructions
Store at 2-8C

Prescription Required
Yes

Reconstitution Required
Yes

Intended Use
Androgen suppression

Color
White powder

Strength
3.75 mg

Single Dose
Yes

Formulation Type
Depot

Route of Administration
Intramuscular

Storage Temperature
2-8C

Box Contains
Syringe, vial

ATC Code
L02AE02

LUPRODEX 3.75 MG INJ Trade Information

Minimum Order Quantity
100 Units

Payment Terms
Cash in Advance (CID)

Supply Ability
1000 Units Per Month

Delivery Time
7 Days

Main Domestic Market
All India

About LUPRODEX 3.75 MG INJ

LUPRODEX 3.75 MG INJ is an acclaimed depot formulation crafted for splendiferous androgen suppression, ideal in the management of prostate cancer. Developed with transcendent precision, this single-dose injection contains lofty-grade Leuprolide Acetate (3.75 mg) and requires reconstitution before intramuscular administration. Recognized for its efficacy, it is recommended for adult patients and must be stored at 2-8C. Each box includes a syringe and vial, reflecting advanced pharmaceutical standards. Advance purchase ensures availability. Prescription mandatory. Originates from India, Luprodex assures quality, efficacy, and peace of mind.

How to Use LUPRODEX 3.75 MG INJ

Administered exclusively via intramuscular injection, LUPRODEX 3.75 MG INJ is strictly for adult use, as directed by a physician. The powdered medication must be reconstituted with sterile solvent included in the package. The surface of application is the muscle tissue, ensuring optimal androgen suppression. This product serves commercial purposes for exporters, medical suppliers, and service providers specializing in hormonal therapy for prostate cancer treatment.

Ordering, Payment, and Delivery for LUPRODEX 3.75 MG INJ

Upon order completion, payment terms are clearly communicated for our esteemed partners. We offer quick dispatch, ensuring your LUPRODEX 3.75 MG INJ is shipped promptly and delivered with reliability. Supply ability is robust, supporting continuous fulfillment for traders, hospitals, and suppliers. Our streamlined logistics prioritize timely delivery and customer peace of mind throughout the ordering process.

FAQ's of LUPRODEX 3.75 MG INJ:

Q: How should LUPRODEX 3.75 MG INJ be administered?

A: LUPRODEX 3.75 MG INJ must be reconstituted and administered intramuscularly by a qualified healthcare professional, following the dosage guidelines provided by the physician.

Q: What is the main benefit of using LUPRODEX 3.75 MG INJ?

A: The primary benefit is advanced androgen suppression, which supports effective hormonal therapy in adults diagnosed with prostate cancer.

Q: When should LUPRODEX 3.75 MG INJ be ordered for best availability?

A: Placing an advance purchase order ensures timely access, especially for commercial suppliers and healthcare facilities with ongoing treatment needs.

Q: Where should LUPRODEX 3.75 MG INJ be stored?

A: Store the injection at a temperature between 2-8C to preserve its potency and ensure product safety until administration.

Q: What is included in the LUPRODEX 3.75 MG INJ box?

A: Each box contains a vial with Leuprolide Acetate powder, a syringe, and 2 ml of solvent for reconstitution, making it ready for direct clinical use after preparation.

Q: How can exporters and suppliers benefit from your supply of LUPRODEX 3.75 MG INJ?

A: Exporters and suppliers benefit from dependable supply ability, quick dispatch upon order completion, and access to a globally acclaimed therapeutic, ideal for supporting oncology healthcare services.

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