Prostacyclin Sodium API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in the formulation of vasodilator and antiplatelet medications. Prostacyclin Sodium (also known as Epoprostenol Sodium) is a synthetic form of prostacyclin (PGI₂), a naturally occurring prostaglandin that acts as a potent vasodilator and inhibitor of platelet aggregation. It is primarily indicated for the treatment of pulmonary arterial hypertension (PAH) and is extensively utilized in cardiovascular, pulmonary, and critical care therapies. Its exceptional purity, stability, and batch-to-batch consistency make it suitable for pharmaceutical formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research applications.
MEDIOCON INC is a trusted Prostacyclin Sodium API manufacturer and bulk supplier in India, supplying premium-quality pharmaceutical ingredients to pharmaceutical companies, biotechnology organizations, contract manufacturing organizations (CMOs), formulation developers, research laboratories, and international distributors. Our GMP-compliant manufacturing facilities employ advanced manufacturing technologies and stringent quality management systems to ensure superior purity, consistency, and compliance with international pharmaceutical standards.
Every batch of Prostacyclin Sodium API manufactured by MEDIOCON INC undergoes comprehensive analytical testing using validated quality control methods. Critical quality parameters including identity, assay, impurity profile, moisture content, pH, melting point, specific rotation, residual solvents, endotoxin levels, particle size distribution, and stability are carefully evaluated before commercial release to ensure compliance with stringent pharmaceutical quality specifications.
Our Prostacyclin Sodium API is available in USP, EP, Research Grade, and Pharmaceutical Grade, making it suitable for injectable formulations, pulmonary hypertension therapies, cardiovascular drug development, analytical testing, formulation development, quality control laboratories, stability studies, and pharmaceutical process validation. We also provide complete regulatory documentation, including Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), Technical Data Sheet (TDS), and supporting regulatory documents, ensuring seamless procurement and regulatory compliance.
With a strong commitment to quality, innovation, and customer satisfaction, MEDIOCON INC has established itself as a dependable global supplier of pharmaceutical raw materials. Through secure cold-chain packaging, competitive pricing, efficient logistics, and dedicated technical support, we ensure reliable worldwide delivery of premium-quality Prostacyclin Sodium API.
If you are looking for a trusted Prostacyclin Sodium API manufacturer, exporter, and bulk supplier, MEDIOCON INC provides pharmaceutical-grade ingredients backed by complete documentation, consistent quality, and timely worldwide supply.
| Parameter | Specification |
|---|---|
| Appearance | White to Off-White Lyophilized Powder |
| Identification | IR, HPLC & UV Complies |
| Assay (HPLC) | 98.0% – 102.0% |
| Loss on Drying | NMT 2.0% |
| Residue on Ignition | NMT 0.2% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 9.5 – 10.5 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 1.5% |
| Water Content | NMT 2.0% |
| Specific Rotation | −48° to −58° (c = 1, Water) |
| Melting Point | 155°C – 165°C |
| Solubility | Freely Soluble in Water; Slightly Soluble in Methanol |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Prostacyclin Sodium API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 61849-14-7) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Prostacyclin Sodium API Manufacturer & Bulk Supplier in India | MEDIOCON INC is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing before release with a Certificate of Analysis.
Export Markets
Quality & Compliance