Losartan Potassium API Manufacturer for South Korea | WHO GMP Certified India

Losartan API — USP / BP / EP with COA | South Korea

Aarise Pharmaceuticals supplies Losartan API for South Korea with full Certificate of Analysis (COA) and WHO GMP documentation. Every batch is tested to USP / BP / EP pharmacopoeial standards at 99%+ (HPLC) purity before dispatch — ensuring your formulation team receives a consistently high-quality, fully documented API from a regulated Indian manufacturer.

Losartan API — Specifications

Below are the key quality and supply parameters for Losartan API supplied by Aarise Pharmaceuticals for South Korea:

About Losartan

Losartan is a pharmaceutical active pharmaceutical ingredient used by formulation manufacturers worldwide. It is used in a wide range of pharmaceutical formulations across therapeutic categories. Aarise Pharmaceuticals manufactures Losartan API at our WHO GMP certified facility in Haridwar, India — one of India’s major pharmaceutical manufacturing hubs — and supplies to formulation companies, distributors, and exporters for South Korea and internationally.

Losartan API Import Requirements for South Korea

Importing Losartan API into South Korea requires compliance with MFDS regulations. Aarise Pharmaceuticals provides the complete documentation package for import authorisation:

• WHO GMP Certificate: Our Haridwar facility holds valid WHO GMP certification accepted by MFDS — the standard required for pharmaceutical API import authorisation in South Korea.
• Certificate of Analysis (COA): Batch-specific COA with full analytical results — required for every shipment for customs clearance.
• Certificate of Pharmaceutical Product (CPP): Issued by India’s CDSCO — required by MFDS for import licence and drug registration applications. Available on request.
• Certificate of Origin: India-origin certificate for customs clearance and preferential tariff treatment under applicable trade agreements.
• MSDS: Material Safety Data Sheet (GHS-compliant) for customs and storage compliance in South Korea.
• Free Sale Certificate: From India’s CDSCO — available on request for South Korea regulatory submissions.

Our regulatory affairs team is experienced in supporting pharmaceutical imports into South Korea and can guide your procurement team through the documentation process.

Why Source Losartan API from Aarise Pharmaceuticals?

Formulation manufacturers for South Korea choose Aarise Pharmaceuticals for Losartan API because of our combination of WHO GMP quality, fast delivery, complete documentation, and competitive pricing. Here is what sets us apart:

• WHO GMP Certified Facility: Our Haridwar manufacturing facility holds valid WHO GMP certification — accepted by CDSCO (India) and regulatory bodies in 18+ export markets including ANVISA (Brazil), INVIMA (Colombia), COFEPRIS (Mexico).
• Consistent 99%+ (HPLC) Purity: Every batch of Losartan API is tested by HPLC before release. Purity results, chromatograms, and full analytical data are included in the batch-specific COA — no batch leaves our facility without QA approval.
• Complete Documentation Package: COA, MSDS, Certificate of Origin, pharmacopoeial compliance statement — all provided as standard. DMF letter of access and CPP available on request for regulatory filings.
• Competitive Pricing: Direct manufacturer pricing with no intermediary markup. Volume discounts from 5kg+. Annual supply agreements with committed pricing available for regular buyers.
• Fast Delivery to South Korea: 3–5 days air / 18–25 days sea. Same-day dispatch available for in-stock APIs.
• Dedicated Export Support: Named account manager for South Korea accounts — quotations within 4 business hours, responsive technical support.

Packaging and Storage

Losartan API is packaged to maintain purity and stability throughout storage and transit to South Korea:

• Primary Packaging: Double-layered aluminium foil bags, heat-sealed, nitrogen-flushed
• Secondary Packaging: HDPE drums or fibre drums
• Available Sizes: 5kg, 25kg aluminium foil bags / HDPE drums
• Storage Conditions: Below 25°C, dry place, protected from light
• Shelf Life: 36 months from manufacture

Who We Supply — Losartan API in South Korea

• Pharmaceutical Manufacturers: Formulation companies producing Losartan-based injectable and specialty pharmaceutical formulations for domestic and export markets
• Pharmaceutical Importers: Licensed importers supplying to formulation companies within South Korea
• Research Institutions and CROs: Losartan API for analytical reference standards, R&D, and formulation feasibility studies
• Export Manufacturers: Companies in South Korea exporting finished Losartan-based formulations to other markets

Pricing and Minimum Order Quantities

• Sample Orders: 100g (sample) — COA, MSDS, and Certificate of Origin included. Sample cost credited against first commercial order.
• Standard Commercial Orders: 5kg commercial — Competitive ex-works pricing. Quote within 4 business hours.
• Bulk Orders: 5kg and above — volume pricing. Annual supply agreements with committed pricing available.
• Payment Terms: TT advance for first orders. 30-day credit for established accounts. USD invoicing for international buyers.

Frequently Asked Questions — Losartan API for South Korea