Mefenamic Capsules

Name: Mefenamic Capsules
Brand: Artemisine Medicines Technology Co., Ltd.

Capsules

Mefenamic Capsules — GMP manufactured capsules by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product Name	Mefenamic Capsules
Dosage Form	Capsules
Strength	250 mg
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▾

Pain and inflammation: dysmenorrhoea, musculoskeletal pain, arthritis, dental and post-operative pain (NSAID class after paracetamol on the WHO analgesic ladder).

💧Administration▾

Oral tablets/capsules with or after food; piroxicam and other long-acting NSAIDs are usually given once or twice daily.

⚖️Dosage▾

Mefenamic acid 500 mg three times daily with food (dysmenorrhoea 500 mg three times daily as needed). Piroxicam 10–20 mg once daily. Use the lowest effective dose; short-course treatment is preferred in the elderly.

⚠️Precautions & Warnings▾

Class risks: GI bleeding/perforation, renal impairment, fluid retention and thrombotic events. Avoid in active ulcer, severe renal or hepatic impairment, heart failure, late pregnancy; avoid combining with other NSAIDs, corticosteroids or anticoagulants.

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.

🛡️

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

Mefenamic Capsules — Frequently Asked Questions

Which documents are provided for Mefenamic Capsules registration?

Every batch of Mefenamic Capsules 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 Mefenamic Capsules?

MOQ and lead time for Mefenamic Capsules 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 Mefenamic Capsules, subject to the regulatory requirements of the destination market.

Which markets have you exported capsules products to?

We have supplied capsules 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 Mefenamic Capsules controlled?

Mefenamic Capsules 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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