Ebastatine Tablets 10mg

Name: Ebastatine Tablets 10mg
Brand: Artemisine Medicines Technology Co., Ltd.

Tablets

Ebastatine (Ebastine) 10mg tablets — a second-generation H1 antihistamine for allergic rhinitis and chronic urticaria. GMP manufactured by Artemisine Medicines Technology with factory-direct pricing and complete registration documentation (COA, COPP, DMF, CTD dossiers) for global export markets.

Product Name	Ebastatine Tablets 10mg
Dosage Form	Tablets
Strength	10 mg
Standards	BP / ENTERPRISE
Packing	10×2 blister (20 tablets per 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▾

Symptomatic relief of allergic rhinitis (seasonal and perennial) and chronic idiopathic urticaria. Second-generation H1-antihistamines are the preferred oral class in WHO-aligned allergy guidance for their favorable safety and low-sedation profile.

💧Administration▾

Oral, once daily, with or without food. Swallow whole — tablets should not be split; take the entire dose.

⚖️Dosage▾

Adults and children 12 years and over: 10 mg once daily.

⚠️Precautions & Warnings▾

Minimal sedation at recommended doses; caution when co-administered with CYP3A4 inhibitors (ketoconazole, erythromycin) and in patients with known QT prolongation. Adjust dose in hepatic impairment. Use in pregnancy only if clearly needed.

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

Ebastatine Tablets 10mg — Frequently Asked Questions

Which documents are provided for Ebastatine Tablets 10mg registration?

Every batch of Ebastatine Tablets 10mg 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 Ebastatine Tablets 10mg?

MOQ and lead time for Ebastatine Tablets 10mg 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 Ebastatine Tablets 10mg, subject to the regulatory requirements of the destination market.

Which markets have you exported tablets products to?

We have supplied tablets 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 Ebastatine Tablets 10mg controlled?

Ebastatine Tablets 10mg 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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