Ceftriaxone 1g Powder for Injection

Name: Ceftriaxone 1g Powder for Injection
Brand: Artemisine Medicines Technology Co., Ltd.

Injection

Ceftriaxone 1g Powder for Injection

Ceftriaxone 1g Powder for 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	Ceftriaxone 1g Powder for Injection
Dosage Form	Injection
Strength	1 g
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▾

WHO first-line injectable for severe pneumonia, meningitis, sepsis and gonorrhoea (ceftriaxone); oral cephalosporins for respiratory and urinary infections.

💧Administration▾

Intravenous or intramuscular (reconstituted, use immediately for IV); oral forms may be given with food.

⚖️Dosage▾

Ceftriaxone adults 1–2 g once daily (2 g daily in meningitis); children 50–80 mg/kg once daily (meningitis up to 100 mg/kg/day). Cefixime adults 200–400 mg daily; children 8 mg/kg/day.

⚠️Precautions & Warnings▾

Cephalosporin or severe penicillin allergy contraindication. Do not mix ceftriaxone with calcium-containing IV solutions in neonates. Monitor for diarrhoea, rash and injection-site reactions.

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.

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GMP Quality

Full batch testing and quality traceability under standard GMP workshops.

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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

Ceftriaxone 1g Powder for Injection — Frequently Asked Questions

Which documents are provided for Ceftriaxone 1g Powder for Injection registration?

Every batch of Ceftriaxone 1g Powder for 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 Ceftriaxone 1g Powder for Injection?

MOQ and lead time for Ceftriaxone 1g Powder for 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 Ceftriaxone 1g Powder for 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 Ceftriaxone 1g Powder for Injection controlled?

Ceftriaxone 1g Powder for 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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