Artemether Injection

● 80 mg artemether per mL — oily solution for intramuscular injection, supplied in 1 mL glass ampoules [1] ● Artemisinin derivative, rapidl

Artemether Injection product packaging
Injection

Artemether Injection

● 80 mg artemether per mL — oily solution for intramuscular injection, supplied in 1 mL glass ampoules [1]
● Artemisinin derivative, rapidly metabolised to the active metabolite dihydroartemisinin [1]
● Fast-acting schizontocide against the asexual blood stages of P. falciparum, with no cross-resistance with chloroquine [1]

Product NameArtemether Injection
Dosage FormInjection
Strength80 mg / 1 mL
StandardsBP / ENTERPRISE
PackingCustomized per market requirement (bottle / blister / box)
DocumentsCOA, COPP, DMF, CTD Dossiers
MOQContact 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▾
● Treatment of severe malaria due to Plasmodium falciparum in adults and children [1] ● To be used when artesunate injection is not available [1] ● Not for malaria prevention and not for uncomplicated malaria [1]
💧Administration▾
● Deep intramuscular injection only — never intravenous [1] ● Strict aseptic technique; use a new syringe and needle for each dose [1] ● In children, inject into the anterior thigh (not the buttocks) [1] ● Give for at least 24 hours, until the patient can take oral medication, then complete with a full course of oral artemisinin-based combination therapy (ACT) [1]
⚖️Dosage▾
Adults 160 mg once (2 × 80 mg ampoules) 80 mg once daily (1 × 80 mg ampoule) Children 3.2 mg/kg once daily 1.6 mg/kg once daily
⚠️Precautions & Warnings▾
● Contraindicated in hypersensitivity to artemether; do not use in peanut or soya allergy (contains peanut oil) [1] ● Pregnancy: use only if absolutely necessary; caution, especially in the first trimester [1] ● May affect the ECG (QTc prolongation) — caution in heart conditions, low blood potassium, or QT-affecting medicines [1] ● Common side effects: pain at the injection site, transient decreases in blood cell counts, bradycardia [1] ● Store below 30 °C, protected from light; do not refrigerate or freeze [1] ● Prescription-only medicine; keep out of the reach of children [1] For full prescribing informatio

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

Artemether Injection — Frequently Asked Questions

Which documents are provided for Artemether Injection registration?

Every batch of Artemether 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 Artemether Injection?

MOQ and lead time for Artemether 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 Artemether 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 Artemether Injection controlled?

Artemether 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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