Antimalarial & Antiprotozoal

Artemether + LumefantrineThird Party Manufacturing in India

Looking to get Artemether + Lumefantrine manufactured under your brand? Our WHO-GMP certified partner facilities support PCD franchise partners and global export opportunities structured across 25+ countries.

WHO-GMP Certified
Export Ready
PCD Franchise Available
CAS Number
141204-94-6
Drug Class
Artemisinin Derivative + Aryl Aminoalcohol (Blood Schizontocides)
Molecular Formula
C₁₆H₂₆O₅ · C₃₀H₃₂Cl₃NO
Molecular Weight
827.3 g/mol
Grade Standards
IP, USP
Therapeutic Category
Antimalarial & Antiprotozoal
MOQ
Contact us for MOQ — varies by strength and dosage form
Dosage Forms
Tablet

Mechanism of Action

Artemether + Lumefantrine works by combining two antimalarial agents with complementary mechanisms of action to target the malaria parasite at different stages of its lifecycle. Artemether, a semi-synthetic artemisinin derivative, acts rapidly in the blood schizont stage. Inside the malaria parasite, the endoperoxide bridge of artemether interacts with intraparasitic iron or heme. This interaction generates highly reactive free radicals that damage and destroy essential parasite proteins and membranes, resulting in a rapid reduction of parasite density.

Lumefantrine, an aryl aminoalcohol, works slower but has a much longer half-life. It acts by preventing the detoxification of heme, a toxic byproduct of hemoglobin digestion by the malaria parasite. By inhibiting the crystallization of heme into non-toxic hemozoin, lumefantrine causes toxic heme to accumulate inside the parasite, leading to its death.

Unlike single-agent therapies, this fixed-dose combination ensures the rapid clearance of parasites by artemether while lumefantrine eradicates any remaining parasites to prevent recrudescence and drug resistance. It is highly effective and well-tolerated for patients with uncomplicated malaria caused by Plasmodium falciparum.

Therapeutic Uses & Indications

Therapeutic Uses

Artemether + Lumefantrine is prescribed for the treatment of:

  • Acute Uncomplicated Malaria: Treating symptomatic malaria infections caused by the Plasmodium falciparum parasite.
  • Drug-Resistant Malaria: Cleaving and eliminating malaria strains that are resistant to older therapies like chloroquine or sulfadoxine-pyrimethamine.
  • Pediatric Malaria Treatment: Formulating specific dosage forms to treat malaria in infants and children weighing over five kilograms.

Why Manufacturers Choose Artemether + Lumefantrine

Artemether + Lumefantrine is the gold standard ACT (Artemisinin-based Combination Therapy) recommended by the World Health Organization (WHO) for the treatment of uncomplicated falciparum malaria. This official endorsement translates to massive, consistent demand from global health organizations, government supply tenders, and private distribution channels, particularly in tropical regions of Africa, Southeast Asia, and Latin America.

For pharmaceutical marketers and third-party contract buyers, adding this combination to their catalog is crucial for establishing authority in the anti-infective therapeutic segment. The combination requires sophisticated formulation expertise to maintain the chemical stability of the fast-acting artemether alongside the slower-releasing lumefantrine. Sourcing this combination from WHO-GMP certified facilities in India allows distributors to benefit from mature supply chains, high-volume production efficiencies, and complete documentation for international regulatory filings.

Dosage Forms We Manufacture

Tablet
20mg + 120mg · 40mg + 240mg · 80mg + 480mg

Frequently Asked Questions

What is the minimum order quantity for Artemether + Lumefantrine?
Minimum order quantity for Artemether + Lumefantrine is Contact us for MOQ — varies by strength and dosage form. Please contact us for bulk pricing and custom quantities.
What dosage forms of Artemether + Lumefantrine can you manufacture?
We manufacture Artemether + Lumefantrine as: Tablet (20mg + 120mg, 40mg + 240mg, 80mg + 480mg).
Are your manufacturing facilities WHO-GMP certified?
Yes. Celesta Healthcare works exclusively with WHO-GMP certified partner production facilities. All manufacturing batches are subject to strict quality control and documentation.
Can you manufacture Artemether + Lumefantrine for export?
Yes. We provide export-ready Artemether + Lumefantrine formulations structured across 25+ countries. We provide full export documentation including Certificate of Analysis (CoA), Certificate of Origin, and regulatory dossiers on request.
What grade standards do you follow for Artemether + Lumefantrine?
We manufacture Artemether + Lumefantrine to IP, USP pharmacopoeial standards.
Third Party Manufacturing

Get Artemether + Lumefantrine made under your brand

  • WHO-GMP certified facilities
  • Quote within 24 hours
  • Low MOQ, export ready
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Our Manufacturing Capabilities

  • WHO-GMP Certified Partner Plants
  • 25+ years of pharma industry experience
  • PCD Franchise with monopoly rights
  • Export support across 25+ countries
  • Small batch to commercial scale
  • Custom formulation development

Packaging Options

Blister pack (Alu-PVC), Strip pack. Customized packaging formats available.

Start Manufacturing Artemether + Lumefantrine Today

Celesta Healthcare provides WHO-GMP certified third-party manufacturing for Artemether + Lumefantrine across all dosage forms. PCD franchise and export orders welcome.

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