Clindamycin Injection

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

Injection

Clindamycin 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	Clindamycin Injection
Dosage Form	Injection
Strength	300 mg/2 mL / 150 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▾

Anaerobic and Gram-positive infections, including bone and joint infections; alternative for penicillin-allergic patients.

💧Administration▾

Oral with a full glass of water (avoid supine immediately after dosing); IM/IV injection for severe infection.

⚖️Dosage▾

Lincomycin adults 500 mg every 8 h oral; clindamycin adults 150–450 mg every 6–8 h oral, severe infection 600–900 mg IV every 8 h. Children 8–25 mg/kg/day divided.

⚠️Precautions & Warnings▾

Pseudomembranous colitis risk — discontinue if significant diarrhoea develops. Monitor hepatic and renal function during prolonged therapy.

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

Clindamycin Injection — Frequently Asked Questions

Which documents are provided for Clindamycin Injection registration?

Every batch of Clindamycin 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 Clindamycin Injection?

MOQ and lead time for Clindamycin 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 Clindamycin 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 Clindamycin Injection controlled?

Clindamycin 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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