Idarubicin Hydrochloride for Injection

1 USD ($)/Box

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Product Details:

Salt Composition Idarubicin Hydrochloride
Dosage Form For Injection
Indication Used in the treatment of Acute Myeloid Leukemia (AML)
Enzyme Types Other
Feature Other
Ingredients Other
Application Other
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Idarubicin Hydrochloride for Injection Price And Quantity

Minimum Order Quantity 100 Box
Price 1 USD ($)/Box

Idarubicin Hydrochloride for Injection Product Specifications

Indication Used in the treatment of Acute Myeloid Leukemia (AML)
Dosage Form For Injection
Salt Composition Idarubicin Hydrochloride
Application Other
Storage Instructions Store at cool and dry place.
Feature Other
Fermentation Smell Odorless
Ingredients Other
Enzyme Types Other
Shelf Life 2 Years
Physical Color/Texture Orange-red lyophilized powder
Ph Level 4.0-5.0 (for reconstituted solution)

Route of Administration Intravenous (IV)
Warning For hospital use only, not for self-administration
Cytotoxicity Cytotoxic agent - handle with care
Prescription Status Rx - prescription only medication
Packaging Type Glass vial with flip-off cap
USP/BP Compliance Meets pharmacopeial standards
Reconstitution Use sterile water for injection
Solubility Soluble in water
Strength 5 mg/vial, 10 mg/vial, 20 mg/vial (varies by manufacturer)

Idarubicin Hydrochloride for Injection Trade Information

FOB Port surat
Payment Terms Cash Against Delivery (CAD), Cash on Delivery (COD), Paypal, Letter of Credit (L/C), Western Union, Letter of Credit at Sight (Sight L/C), Telegraphic Transfer (T/T), Delivery Point (DP), Days after Acceptance (DA), Cash in Advance (CID), Cheque, Cash Advance (CA)
Supply Ability 1000000 Box Per Month
Delivery Time 4 Days
Sample Policy Contact us for information regarding our sample policy
Packaging Details 1 Vial
Main Export Market(s) Western Europe, North America, South America, Middle East, Central America, Eastern Europe, Asia, Australia, Africa
Main Domestic Market Himachal Pradesh, Andaman and Nicobar Islands, Nagaland, Uttarakhand, Daman and Diu, Dadra and Nagar Haveli, Lakshadweep, South India, North India, East India, West India, Assam, Arunachal Pradesh, Bihar, Chandigarh, Delhi, Gujarat, Goa, Haryana, Jammu and Kashmir, Jharkhand, Karnataka, Madhya Pradesh, Maharashtra, Mizoram, Meghalaya, Manipur, Punjab, Pondicherry, Rajasthan, Sikkim, Tamil Nadu, Telangana, Tripura, Uttar Pradesh, West Bengal, Andhra Pradesh, Kerala, Central India, Odisha, Chhattisgarh, All India
Certifications ISO/GMP/c-GMP/WHOGMP/USFDA/EUGMP.

Product Description

Since last manyyears SaintroyLifescienceis leading manufacture, export and supplierofIdarubicin Hydrochloride for Injectionfrom Surat, Gujarat, India. Idarubicin Hydrochloride for Injection used for treatment of acute lymphoblastic leukemia and chronic myelogenous leukemia in blast crisis.

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ISO/GMP/cGMP/WHOGMP/NAFDAC approved, PPB Kenya approved/USFDA approved/EUGMP approved/MOH Iran approved manufacturingfacility in Gujarat, India.

Registration: Saintroy Lifescienceis interested in registrationof own brand or customer brands in ministryof health of clientscountry and we also provide the products samples, COA, COPP, ACTD or CTD dossier, DMF, Manufacturing license, Free sales certificate and other required documents.

Export Country:Saintroy Lifescience Idarubicin Hydrochloridefor Injection export to USA, Canada, Germany, Europe, France,Ghana, Nigeria, Kenya, Senegal, Sudan,UAE, Kuwait, Dubai, Cameroon, Lebanon,Peru, Chile, Somalia, Philippines, Myanmar, Maldives, Thailand, Singapore,Malaysia, Hong Kong, China, Zimbabwe, Togo, Burkina Faso, Niger,Guinea Bissau,Congo, Democratic of republic, Ivory Costa, Oman, Guatemala, Nicaragua,Salvador, Qatar, Costa Rica, Panama, Cuba, Colombia, Bolivia, Argentine,Algeria, Guyana, Morocco, Jordan, Bahrain, Iran, Egypt, Kyrgyzstan, Uzbekistan,Kazakhstan.

Effective Treatment for AML

Idarubicin Hydrochloride for Injection is a vital therapy in the management of Acute Myeloid Leukemia (AML). Its cytotoxic activity targets rapidly dividing cells, offering significant benefits in remission induction when administered as recommended by clinical protocols. The product is supplied in reliable glass vials, supporting stable dosage and consistent efficacy.

Strict Quality Compliance and Safety

This medication meets stringent USP/BP pharmacopeial standards, ensuring patients and providers receive a high-quality pharmaceutical product. As a cytotoxic agent, professionals must handle it with caution, adhering to all hospital safety guidelines. The flip-off cap packaging enhances secure access and reduces contamination risk during preparation.

FAQ's of Idarubicin Hydrochloride for Injection:

Q: How is Idarubicin Hydrochloride for Injection prepared and administered?

A: The powder must be reconstituted with sterile water for injection, yielding a solution with a pH of 4.0-5.0. It is then administered intravenously by healthcare professionals only, not for self-administration.

Q: What is the primary indication for using Idarubicin Hydrochloride for Injection?

A: This medication is indicated for the treatment of Acute Myeloid Leukemia (AML), providing an effective cytotoxic option as part of a hospital-administered chemotherapy protocol.

Q: When should Idarubicin Hydrochloride for Injection be used?

A: Idarubicin should only be employed under medical supervision, typically within the structured schedules of oncology treatment centers based on a physician's guidance.

Q: Where should this medication be stored and prepared?

A: Store this product in a cool, dry location as directed. Reconstitution and preparation must occur in a hospital or approved clinical setting with appropriate cytotoxic handling protocols.

Q: What are the safety precautions for handling Idarubicin Hydrochloride?

A: Handle as a cytotoxic agent, wearing protective equipment and ensuring all preparation occurs in designated hospital areas to minimize exposure and environmental risk.

Q: What benefits does Idarubicin Hydrochloride offer in cancer treatment?

A: Idarubicin Hydrochloride provides targeted action against malignant cells in AML, contributing to remission rates and improving patient outcomes under strict medical supervision.

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