Acetylcysteine Injection

Name: Acetylcysteine Injection
Brand: Artemisine Medicines Technology Co., Ltd.

Injection

Acetylcysteine 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	Acetylcysteine Injection
Dosage Form	Injection
Strength	1 g/5 mL / 200 mg/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▾

Adjunct in oxidative stress-related conditions, hepatic support and detoxification protocols; acetylcysteine is the WHO-listed antidote for paracetamol poisoning and mucolytic in respiratory disease.

💧Administration▾

Oral tablets/sachets, or intravenous infusion for acute poisoning and severe indications.

⚖️Dosage▾

Acetylcysteine (paracetamol poisoning): 150 mg/kg IV over 1 hour, then 50 mg/kg over 4 hours, then 100 mg/kg over 16 hours — as per protocol. Oral mucolytic 200 mg 2–3 times daily. Glutathione supplements usually 600–1200 mg daily per label.

⚠️Precautions & Warnings▾

Intravenous acetylcysteine may cause anaphylactoid reactions — monitor during infusion. Supplement use should not replace evidence-based therapy; consult a clinician for hepatic disease.

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

Acetylcysteine Injection — Frequently Asked Questions

Which documents are provided for Acetylcysteine Injection registration?

Every batch of Acetylcysteine 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 Acetylcysteine Injection?

MOQ and lead time for Acetylcysteine 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 Acetylcysteine 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 Acetylcysteine Injection controlled?

Acetylcysteine 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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