Quinagolide Hydrochloride API is a premium-quality pharmaceutical-grade Active Pharmaceutical Ingredient (API) widely used in endocrinology and neuropharmaceutical formulations. Quinagolide Hydrochloride is a selective dopamine D2 receptor agonist primarily indicated for the treatment of hyperprolactinemia, including prolactin-secreting pituitary adenomas (prolactinomas), menstrual disorders, infertility associated with elevated prolactin levels, and galactorrhea. Its superior purity, chemical stability, and batch-to-batch consistency make it ideal for pharmaceutical formulation development, analytical testing, quality control, stability studies, and authorized pharmaceutical research applications.
MEDIOCON INC is a trusted Quinagolide Hydrochloride 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 global distributors. Our GMP-compliant manufacturing facilities employ advanced manufacturing technologies and stringent quality management systems to ensure exceptional purity, consistency, and compliance with international pharmaceutical standards.
Every batch of Quinagolide Hydrochloride 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, particle size distribution, heavy metals, and stability are carefully evaluated before commercial release to ensure compliance with stringent pharmaceutical specifications.
Our Quinagolide Hydrochloride API is available in USP, EP, Research Grade, and Pharmaceutical Grade, making it suitable for endocrine formulations, dopamine agonist research, analytical testing, formulation development, quality control laboratories, stability studies, process validation, and pharmaceutical research. 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 packaging, competitive pricing, efficient logistics, and responsive technical support, we ensure reliable worldwide delivery of premium-quality Quinagolide Hydrochloride API.
If you are looking for a trusted Quinagolide Hydrochloride 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 Crystalline Powder |
| Identification | IR, HPLC & UV Complies |
| Assay (HPLC) | 98.0% – 102.0% |
| Loss on Drying | NMT 0.5% |
| Residue on Ignition | NMT 0.2% |
| Heavy Metals | NMT 10 ppm |
| pH (1% Solution) | 4.5 – 6.5 |
| Individual Impurity | NMT 0.5% |
| Total Impurities | NMT 1.0% |
| Water Content | NMT 1.0% |
| Specific Rotation | −32° to −38° (c = 1, Methanol) |
| Melting Point | 208°C – 214°C |
| Solubility | Freely Soluble in Water and Methanol; Slightly Soluble in Ethanol |
Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Quinagolide Hydrochloride API Manufacturer & Bulk Supplier in India | MEDIOCON INC (CAS 85747-04-8) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.
Our Quinagolide Hydrochloride 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.
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