Taurine Eye Drops

Taurine Eye Drops 5 — GMP manufactured ophthalmic by Artemisine Medicines Technology. Original manufacturer supply with stable quality, fact

Taurine Eye Drops product packaging
Ophthalmic

Taurine Eye Drops

Taurine Eye Drops 5 — GMP manufactured ophthalmic by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product NameTaurine Eye Drops
Dosage FormOphthalmic
Strength5% (50 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▾
Topical ophthalmic treatment as stated on the product label — infection, inflammation or ocular surface support (see the registered indication for your market).
💧Administration▾
Instil into the conjunctival sac using aseptic technique; discard the container 4 weeks after first opening and never share eye drops between patients.
⚖️Dosage▾
Usually 1–2 drops 3–4 times daily, or as directed by the prescriber; follow the product insert for the specific active substance.
⚠️Precautions & Warnings▾
For topical ocular use only. Stop and seek advice if pain, worsening vision or persistent redness develops; avoid contact lenses during treatment.

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

Taurine Eye Drops — Frequently Asked Questions

Which documents are provided for Taurine Eye Drops registration?

Every batch of Taurine Eye Drops 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 Taurine Eye Drops?

MOQ and lead time for Taurine Eye Drops 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 Taurine Eye Drops, subject to the regulatory requirements of the destination market.

Which markets have you exported ophthalmic products to?

We have supplied ophthalmic 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 Taurine Eye Drops controlled?

Taurine Eye Drops 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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