Decitabine For Injection

1 USD ($)/Box

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Product Details:

Salt Composition Decitabine
Dosage Form Lyophilized Powder for Injection
Indication Treatment of Myelodysplastic Syndromes (MDS), including previously treated and untreated, de novo and secondary MDS of all French-American-British subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups
Enzyme Types Other
Feature Other
Ingredients Other
Application Other
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Decitabine For Injection Price And Quantity

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

Decitabine For Injection Product Specifications

Enzyme Types Other
Feature Other
Dosage Form Lyophilized Powder for Injection
Shelf Life 2 Years
Indication Treatment of Myelodysplastic Syndromes (MDS), including previously treated and untreated, de novo and secondary MDS of all French-American-British subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups
Application Other
Physical Color/Texture White to off-white Lyophilized Powder
Storage Instructions Store at cool and dry place.
Fermentation Smell Normal Smell
Ingredients Other
Salt Composition Decitabine

Compatibility Compatible with sterile water for injection
Packaging Type Single-dose vial
Route of Administration Intravenous infusion
Regulatory Approval Marketed under regulatory approval for oncology use
Prescription Status Prescription only
Strength 50 mg/vial
Instructions for Handling Handle under aseptic conditions; use immediately after reconstitution or within recommended time if stored as specified
Reconstitution To be reconstituted with sterile water for injection
Purity Pharmaceutical grade; complies with pharmacopeia standards

Decitabine For Injection Trade Information

FOB Port surat
Payment Terms Cash on Delivery (COD), Days after Acceptance (DA), Delivery Point (DP), Letter of Credit (L/C), Letter of Credit at Sight (Sight L/C), Western Union, Paypal, Cash Against Delivery (CAD), Telegraphic Transfer (T/T), 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) Australia, North America, Eastern Europe, Western Europe, Middle East, Africa, Central America, South America, Asia
Main Domestic Market Dadra and Nagar Haveli, Himachal Pradesh, Nagaland, Uttarakhand, Daman and Diu, Lakshadweep, All India, South India, North India, East India, West India, Andaman and Nicobar Islands, Assam, Arunachal Pradesh, Bihar, Delhi, Goa, Chandigarh, Jammu and Kashmir, Jharkhand, Karnataka, Maharashtra, Mizoram, Meghalaya, Manipur, Pondicherry, Rajasthan, Sikkim, Tamil Nadu, Telangana, Tripura, West Bengal, Gujarat, Madhya Pradesh, Haryana, Punjab, Andhra Pradesh, Kerala, Central India, Odisha, Chhattisgarh, Uttar Pradesh
Certifications ISO/GMP/c-GMP/WHOGMP/USFDA/EUGMP.

Product Description

Since last manyyears Saintroy Lifescience is leading manufacture, export and supplierofDecitabine for Injectionfrom Surat, Gujarat, India. Decitabine forInjection used to treat myelodysplastic syndromes (MDS) including previously treated and untreated, de novo and secondary MDS of all French-American-British Subtypes.

Tags: Decitabine for Injection manufacturer, Decitabine forInjection exporter, Decitabine for Injection supplier, and Decitabine forInjection, whogmp approved Decitabine for Injection manufacturer and supplier, Decitabine ForInjection distributor, Decitabine for Injection shipper, Decitabine forInjection30 mgDecitabine for Injection 30 mg supplier,Decitabine for Injection30 mg.

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

Registration: Saintroy Lifescience is interested inregistration of own brand or customer brands in ministry of 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 Decitabine forInjection 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, HongKong, 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.

Targeted Oncology Solution for MDS

Decitabine For Injection is designed for adults diagnosed with Myelodysplastic Syndromes (MDS), including previously untreated and treated cases, as well as primary and secondary MDS. Its compatibility with a broad spectrum of MDS prognostic subtypes makes it a widely used option within oncology settings.

Reliable Quality and Purity Standards

Manufactured to pharmaceutical-grade standards, Decitabine For Injection ensures high purity and compliance with pharmacopeia guidelines. Its regulatory approval for oncology therapy highlights scrutinized safety, efficacy, and robust manufacturing controls from dealer and manufacturer to end-user.

Simple Preparation and Administration Process

Each vial is reconstituted with sterile water for injection under aseptic conditions. After preparation, immediate use is recommended, though it may be used within a specified window if stored as directed. This ensures product integrity and optimal therapeutic results when administered via intravenous infusion.

FAQ's of Decitabine For Injection:

Q: How should Decitabine For Injection be reconstituted and administered?

A: Decitabine For Injection must be reconstituted only with sterile water for injection under aseptic conditions. After dissolving the powder, administer the dose intravenously as an infusion, following your healthcare provider's instructions.

Q: What is the primary indication for Decitabine For Injection?

A: This product is indicated for the treatment of Myelodysplastic Syndromes (MDS), covering both de novo and secondary cases, and all risk groups specified by the International Prognostic Scoring System.

Q: When should the reconstituted vial be used?

A: The reconstituted solution should be used immediately. If not used promptly, it may be stored for a short period as specified in the product guidelines, but prolonged storage can compromise its quality and efficacy.

Q: Where should Decitabine For Injection be stored before reconstitution?

A: Store the vial in a cool, dry place as recommended on the packaging to maintain its shelf life of up to two years before reconstitution.

Q: What are the benefits of pharmaceutical-grade Decitabine For Injection?

A: Pharmaceutical-grade Decitabine meets strict purity and quality standards, ensuring reliable efficacy and safety for patients undergoing oncology treatment under prescription.

Q: How is Decitabine For Injection supplied and distributed in India?

A: The product is supplied in single-dose vials by authorized dealers, distributors, exporters, manufacturers, suppliers, traders, and wholesalers throughout India, ensuring availability in regulated oncology care settings.

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