Cimetidine Injection

Cimetidine Injection — GMP manufactured injection by Artemisine Medicines Technology. Original manufacturer supply with stable quality, fact

Cimetidine Injection product packaging
Injection

Cimetidine Injection

Cimetidine 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 NameCimetidine Injection
Dosage FormInjection
Strength400 mg/2 mL / 200 mg/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▾
Reduction of gastric acid in peptic ulcer disease, reflux oesophagitis, stress-ulcer prophylaxis and pre-anaesthetic aspiration risk (H2 blockers).
💧Administration▾
Intravenous injection or slow infusion (injectable forms) or oral administration in stable patients.
⚖️Dosage▾
Cimetidine 200–400 mg IV/oral every 6–8 h (max 2.4 g/day); reduce dose in renal impairment. Monitor for accumulation in elderly patients.
⚠️Precautions & Warnings▾
Cimetidine inhibits hepatic enzymes — many drug interactions (warfarin, phenytoin, theophylline); short courses are preferred. Avoid rapid IV bolus; watch for confusion in the elderly and renal impairment.

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

Cimetidine Injection — Frequently Asked Questions

Which documents are provided for Cimetidine Injection registration?

Every batch of Cimetidine 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 Cimetidine Injection?

MOQ and lead time for Cimetidine 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 Cimetidine 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 Cimetidine Injection controlled?

Cimetidine 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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