Heparin Sodium Injection

Name: Heparin Sodium Injection
Brand: Artemisine Medicines Technology Co., Ltd.

Injection

Heparin Sodium Injection — GMP manufactured injection by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product Name	Heparin Sodium Injection
Dosage Form	Injection
Strength	2500IU/mL
Standards	BP / ENTERPRISE
Packing	Customized per market requirement (bottle / blister / box)
Documents	COA, COPP, DMF, CTD Dossiers
MOQ	Contact us for MOQ and current stock

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WHO Prescribing Guidance

Indications · Administration · Dosage · Precautions

Reference information summarised from WHO prescribing guidance. Expand each item below — clinical use must always follow the locally approved product insert.

🎯Indications▾

Prevention and treatment of venous thromboembolism, pulmonary embolism, acute coronary syndromes and extracorporeal circulation (WHO essential medicine for unfractionated heparin).

💧Administration▾

IV bolus/infusion or subcutaneous injection; enoxaparin/other LMWHs are given subcutaneously. Rotate injection sites and do not aspirate or massage.

⚖️Dosage▾

Unfractionated heparin: prophylaxis 5,000 units SC every 8–12 h; treatment by weight-based IV infusion with aPTT monitoring. Enoxaparin prophylaxis 20–40 mg SC once daily. Adjust for renal impairment.

⚠️Precautions & Warnings▾

Bleeding risk — monitor platelet counts (heparin-induced thrombocytopenia), and avoid in active bleeding, severe thrombocytopenia or recent neurosurgery. Protamine sulfate is the antidote for heparin; warfarin requires INR monitoring.

Reference: WHO Model Formulary / WHO Model List of Essential Medicines. For professional reference only — clinical use must follow the locally approved product insert and national treatment guidelines.

Why Order From Us

Factory Direct. Fully Documented.

🛡️

GMP Quality

Full batch testing and quality traceability under standard GMP workshops.

🚢

Fast Delivery

Sufficient stock on regular items, familiar with export logistics to 50+ countries.

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Registration Support

COA, DMF, dossier and legalization documents for your market registration.

FAQ

Heparin Sodium Injection — Frequently Asked Questions

Which documents are provided for Heparin Sodium Injection registration?

Every batch of Heparin Sodium Injection ships with a Certificate of Analysis (COA). For market registration we provide COPP, DMF and CTD-format dossiers, plus legalisation support where your authority requires it.

What is the MOQ and lead time for Heparin Sodium Injection?

MOQ and lead time for Heparin Sodium Injection depend on strength, packaging and destination market. Send us your target market and annual volume — our export team confirms current stock, MOQ and lead time within 24 hours.

Do you support OEM / private label?

Yes. We offer OEM packaging and private-label production for Heparin Sodium Injection, subject to the regulatory requirements of the destination market.

Which markets have you exported injection products to?

We have supplied injection products to 50+ countries across Africa, Southeast Asia, Latin America and the Middle East, with experience in ministry-of-health registration and international tenders.

How is the quality of Heparin Sodium Injection controlled?

Heparin Sodium Injection is produced in China-GMP workshops (site re-inspected and passed in 2026), released only after full QC testing against BP / enterprise standards, with retained samples kept for one year beyond the product's expiry date.

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