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DECADURE 400mg/mL (Nandrolone Decanoate Injection)
DECADURE 400mg/mL contains Nandrolone Decanoate 400mg/mL, a long-acting injectable anabolic steroid. Nandrolone Decanoate is a prescription medication that has approved medical uses in some countries for selected conditions under specialist supervision. It should only be used when prescribed by a qualified healthcare professional and according to local regulatory requirements.
Key Benefits
Long-acting injectable formulation of Nandrolone Decanoate 400mg/mL
Administered via intramuscular injection
Gradual release of the active ingredient over time
Prescription-only medication
Intended for use under medical supervision
Medical Uses
Where approved, Nandrolone Decanoate may be prescribed by healthcare professionals for selected medical conditions, including:
Certain types of anemia
Conditions associated with severe muscle wasting (as determined by a physician)
Other approved therapeutic indications according to local prescribing guidelines
DECADURE 400mg/mL should not be used for bodybuilding, athletic performance enhancement, or non-medical purposes.
How DECADURE 400mg/mL Works
Nandrolone Decanoate is an anabolic steroid that is slowly released after intramuscular injection. It promotes protein synthesis and supports nitrogen retention in the body. Its clinical use should always be based on a physician's assessment of the patient's medical condition, expected benefits, and potential risks.
How to Use
Use only under the supervision of a qualified healthcare provider.
Administer by intramuscular injection according to the prescribed schedule.
Do not exceed the prescribed dose.
Regular follow-up and laboratory monitoring may be required during treatment.
Possible Side Effects
Like all medicines, DECADURE 400mg/mL may cause side effects, including:
Injection-site pain or irritation
Acne or oily skin
Fluid retention
Increased blood pressure
Changes in cholesterol levels
Mood changes
Increased body hair growth
Menstrual irregularities and virilization in females
Suppression of natural testosterone production in males
Seek immediate medical attention if you experience severe allergic reactions, chest pain, difficulty breathing, or signs of a blood clot.
Precautions
Prescription-only medicine.
Use only as directed by a healthcare professional.
Not recommended during pregnancy or breastfeeding.
Inform your doctor if you have heart disease, liver disease, kidney disease, prostate disorders, or a history of blood clots.
Athletes should note that Nandrolone is prohibited by most anti-doping organizations and may result in a positive doping test.
Misuse or abuse of anabolic steroids may lead to serious cardiovascular, hormonal, psychiatric, and liver-related complications.
Storage
Store below 25Β°C in a cool, dry place.
Protect from direct sunlight.
Do not freeze.
Keep out of reach of children.
Frequently Asked Questions (FAQs)
1. What is DECADURE 400mg/mL used for?
DECADURE 400mg/mL contains Nandrolone Decanoate, which may be prescribed in certain countries for specific medical conditions such as selected forms of anemia or muscle-wasting disorders under specialist supervision.
2. How is DECADURE 400mg/mL administered?
It is administered as an intramuscular injection by or under the supervision of a qualified healthcare professional.
3. Is DECADURE 400mg/mL suitable for bodybuilding?
No. It is intended for medically approved uses only. Using anabolic steroids for bodybuilding or athletic performance enhancement carries significant health risks and is not recommended.
4. Does DECADURE 400mg/mL require a prescription?
Yes. Nandrolone Decanoate is a prescription medication and should only be used under medical supervision.
5. How should DECADURE 400mg/mL be stored?
Store below 25Β°C, away from heat, moisture, and direct sunlight. Keep out of the reach of children.
Why Choose DECADURE 400mg/mL?
DECADURE 400mg/mL provides a high-strength Nandrolone Decanoate injectable formulation intended for appropriate prescription medical use where approved. When used under the guidance of a qualified healthcare professional, it offers a long-acting treatment option for selected clinical conditions while supporting careful monitoring for safety and effectiveness.
Zupanib Tablets (Pazopanib Tablets) β Product Description
Zupanib Tablets contain Pazopanib, a prescription targeted anti-cancer medicine used to treat advanced renal cell carcinoma (RCC) and advanced soft tissue sarcoma (STS). It belongs to the tyrosine kinase inhibitor (TKI) class and works by blocking multiple enzymes involved in tumor growth and the formation of new blood vessels (angiogenesis), helping slow the progression of cancer.
Zupanib is taken orally once daily, usually on an empty stomach, exactly as prescribed by the treating oncologist. It may be used as a single-agent therapy depending on the patient's diagnosis and treatment plan.
Active Ingredient
Pazopanib
Dosage Form
Oral Tablets
Therapeutic Indications
Advanced Renal Cell Carcinoma (Kidney Cancer)
Advanced Soft Tissue Sarcoma (STS)
Other approved oncology indications as determined by the treating oncologist
How It Works
Pazopanib inhibits multiple tyrosine kinase receptors, including VEGFR, PDGFR, and c-KIT, reducing the formation of new blood vessels that supply tumors with oxygen and nutrients. This helps inhibit tumor growth and spread.
Key Features
Targeted therapy for advanced kidney cancer and soft tissue sarcoma
Multi-targeted kinase inhibitor with anti-angiogenic activity
Convenient once-daily oral tablet
May help slow disease progression in eligible patients
Manufactured according to stringent pharmaceutical quality standards
Storage
Store below 30Β°C in a cool, dry place.
Protect from moisture and direct sunlight.
Keep out of reach of children.
Note: Zupanib Tablets (Pazopanib) are prescription-only medicines and should be used only under the supervision of a qualified oncologist. Regular monitoring of liver function, blood pressure, thyroid function, and overall clinical status is recommended during treatment.
Zucarfil (Carfilzomib Injection 60 mg) β Product Description
Zucarfil contains Carfilzomib 60 mg, a targeted anti-cancer medicine used for the treatment of relapsed or refractory multiple myeloma (RRMM). It belongs to the proteasome inhibitor class of medicines and works by irreversibly blocking the 20S proteasome, causing the accumulation of damaged proteins within cancer cells. This leads to cellular stress and programmed cancer cell death (apoptosis), helping slow disease progression.
Zucarfil is supplied as a lyophilized powder for intravenous (IV) infusion and is administered by qualified healthcare professionals. It is commonly used in combination with medicines such as dexamethasone, lenalidomide, or daratumumab, depending on the patient's treatment regimen and clinical condition.
Active Ingredient
Carfilzomib 60 mg
Dosage Form
Lyophilized Powder for Injection (IV Infusion)
Therapeutic Indications
Relapsed Multiple Myeloma
Refractory Multiple Myeloma
Multiple Myeloma Combination Therapy
Other approved indications as determined by the treating oncologist
How It Works
Carfilzomib selectively and irreversibly inhibits the 20S proteasome, preventing the breakdown of unwanted proteins inside cancer cells. The resulting protein buildup disrupts normal cell function, triggering apoptosis and reducing the growth of multiple myeloma cells.
Key Features
Targeted proteasome inhibitor for multiple myeloma
Effective in relapsed and refractory disease
Administered by intravenous infusion under specialist supervision
Commonly used in combination with established myeloma therapies
Manufactured according to stringent pharmaceutical quality standards
Storage
Store refrigerated at 2Β°Cβ8Β°C.
Protect from light and do not freeze.
Keep out of reach of children.
Note: Zucarfil (Carfilzomib Injection 60 mg) is a prescription-only medicine and should be administered only by qualified healthcare professionals experienced in oncology. Patients should be monitored regularly for blood counts, kidney function, liver function, cardiac status, and infusion-related reactions throughout treatment.
Zucarb (Carboplatin Injection) β Product Description
Zucarb contains Carboplatin, a prescription platinum-based chemotherapy medicine used in the treatment of various solid tumors, including ovarian cancer, lung cancer, head and neck cancer, and other malignancies. It belongs to the platinum-containing antineoplastic agents and works by damaging the DNA of cancer cells, preventing their growth and division, ultimately leading to cancer cell death.
Zucarb is administered as an intravenous (IV) infusion by qualified healthcare professionals. It may be used alone or in combination with other chemotherapy medicines depending on the type and stage of cancer, as well as the patient's overall treatment plan.
Active Ingredient
Carboplatin
Dosage Form
Sterile Injection for Intravenous (IV) Infusion
Therapeutic Indications
Ovarian Cancer
Non-Small Cell Lung Cancer (NSCLC)
Small Cell Lung Cancer (SCLC)
Head and Neck Cancer
Endometrial Cancer
Other solid tumors as recommended by the treating oncologist
How It Works
Carboplatin forms DNA cross-links within cancer cells, preventing DNA replication and repair. This disrupts cell division and triggers the death of rapidly dividing cancer cells, helping to slow or stop tumor growth.
Key Features
Platinum-based chemotherapy with proven clinical efficacy
Effective against a wide range of solid tumors
Suitable for use as monotherapy or combination chemotherapy
Administered under specialist oncology supervision
Manufactured according to stringent pharmaceutical quality standards
Storage
Store according to the manufacturer's recommendations.
Protect from excessive heat, freezing, and direct light.
Keep out of reach of children.
Note: Zucarb (Carboplatin Injection) is a prescription-only chemotherapy medicine and should only be administered by qualified healthcare professionals experienced in oncology. Regular monitoring of blood counts, kidney function, liver function, andelectrolyte levels is recommended throughout treatment.