Erlotinib Hydrochloride Tablets

Erlotinib Hydrochloride Tablets — GMP manufactured tablets by Artemisine Medicines Technology. Original manufacturer supply with stable qual

Erlotinib Hydrochloride Tablets product packaging
Tablets

Erlotinib Hydrochloride Tablets

Erlotinib Hydrochloride Tablets — GMP manufactured tablets by Artemisine Medicines Technology. Original manufacturer supply with stable quality, factory direct price and full batch documentation for global markets.

Product NameErlotinib Hydrochloride Tablets
Dosage FormTablets
Strength150 mg
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▾
Selected solid tumours and haematological malignancies (renal cell carcinoma, NSCLC with activating EGFR mutations, gastrointestinal stromal tumours) — use according to molecular testing and oncology protocol.
💧Administration▾
Oral once daily with or without food (follow the specific product's instructions); pemetrexed is given as an intravenous infusion with folate and vitamin B12 supplementation. Swallow tablets whole.
⚖️Dosage▾
Dose is indication-specific and administered under oncologist supervision, e.g. gefitinib 250 mg once daily; erlotinib 150 mg once daily; imatinib 400 mg once daily; afatinib 40 mg once daily; pemetrexed 500 mg/m² every 3 weeks. Dose reduction is required for toxicity.
⚠️Precautions & Warnings▾
Significant toxicity: rash, diarrhoea, hepatic enzyme elevation, interstitial lung disease and QT prolongation; teratogenic — effective contraception required. Monitor blood counts, liver and kidney function, and electrolytes regularly; target-therapy must not be self-managed.

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.

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