Metoclopramide Injection

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

Metoclopramide Injection product packaging
Injection

Metoclopramide Injection

Metoclopramide 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 NameMetoclopramide Injection
Dosage FormInjection
StrengthAs per BP monograph / enterprise standard
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▾
Nausea and vomiting of various causes, including chemotherapy- or radiotherapy-induced emesis, migraine and post-operative nausea.
💧Administration▾
Oral tablets/syrup, orodispersible film, or intravenous/intramuscular injection for acute emesis.
⚖️Dosage▾
Ondansetron adults 4–8 mg every 8–12 h (chemotherapy per protocol); children 0.1–0.15 mg/kg per dose. Metoclopramide adults 10 mg up to three times daily, maximum 5 days.
⚠️Precautions & Warnings▾
Both may prolong QT — avoid with other QT-prolonging drugs. Metoclopramide can cause extrapyramidal reactions, especially in young patients — do not exceed 5 days or 0.5 mg/kg/day. Caution in Parkinson's 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

Metoclopramide Injection — Frequently Asked Questions

Which documents are provided for Metoclopramide Injection registration?

Every batch of Metoclopramide 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 Metoclopramide Injection?

MOQ and lead time for Metoclopramide 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 Metoclopramide 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 Metoclopramide Injection controlled?

Metoclopramide 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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