Finerenone 20 Mg Tablets

Finerenone 20 Mg Tablets — GMP manufactured tablets by Artemisine Medicines Technology. Original manufacturer supply with stable quality, fa

Finerenone 20 Mg Tablets product packaging
Tablets

Finerenone 20 Mg Tablets

Finerenone 20 Mg 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 NameFinerenone 20 Mg Tablets
Dosage FormTablets
Strength20 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▾
Type 2 diabetes mellitus as monotherapy or add-on according to national guidance; finerenone for chronic kidney disease associated with type 2 diabetes.
💧Administration▾
Oral; repaglinide is taken 15–30 minutes before meals and skipped if a meal is skipped. SGLT2 inhibitors are taken once daily, usually in the morning.
⚖️Dosage▾
Repaglinide 0.5–4 mg per meal (max 16 mg/day). SGLT2 inhibitors e.g. ertugliflozin 5–15 mg once daily. Finerenone 10–20 mg once daily based on renal function and potassium. Adjust in renal/hepatic impairment.
⚠️Precautions & Warnings▾
Repaglinide and glinides cause hypoglycaemia — take with a meal. SGLT2 inhibitors: genital infections, volume depletion, euglycaemic ketoacidosis (stop before surgery). Finerenone: monitor potassium and renal function — avoid in hyperkalaemia.

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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Full batch testing and quality traceability under standard GMP workshops.

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Registration Support

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