Sobre Changzhou Ruiming Pharmaceutical Co., Ltd.

Changzhou Ruiming Pharmaceutical Co., Ltd. is located at No.1558 Longjiang North Road, Chunjiang Town, Xinbei District, Changzhou City, Jiangsu Province. Founded in 2005, it is a pharmaceutical enterprise specializing in the R&D, production and sales of pharmaceutical intermediates, active pharmaceutical ingredients (APIs) and preparations related to cardiovascular, urinary, respiratory and digestive systems.

The company is adjacent to the Shanghai–Nanjing Expressway with convenient transportation and superior environment. It manufactures APIs as specified in its Drug Production License. The production scope covers APIs (Propafenone Hydrochloride, Tamsulosin Hydrochloride, Felodipine, Amlodipine Besilate, Levoamlodipine Besylate).

Covering an area of 25,000 square meters, the company is equipped with synthesis workshops, final purification, drying & packaging workshops (GMP-compliant), liquid raw material warehouses, solid raw material warehouses, intermediate warehouses and finished product warehouses, etc.

The company owns two API production lines and one solid preparation production line. The production process equipment and quality testing instruments deployed meet the current requirements of domestic pharmaceutical production and quality management specifications, capable of supporting production and quality control for existing products.

To date, the company has six APIs with registration status “A” that have passed GMP compliance inspections. Among them, Amlodipine Besilate has obtained certifications from EDQM (European Directorate for the Quality of Medicines & HealthCare) and Japan PMDA; Tamsulosin Hydrochloride has passed FDA on-site inspection.
In 2024, the company obtained the marketing approval for Levoamlodipine Besylate Tablets.
It was awarded the title of “Gazelle Enterprise in the Southern Jiangsu National Independent Innovation Demonstration Zone” in 2019, and recognized as a national-level Specialized, Refined, Differential and Innovative (SRDI) “Little Giant” enterprise in 2024.

The production lines for the audited material Amlodipine Besilate include the synthesis workshop and the final purification, drying & packaging workshop, mainly for formulation projects.
Major production equipment includes amlodipine base hydrolysis reactors, amlodipine besilate salt-forming reactors, centrifuges, decolorization reactors, crystallization reactors, double cone rotary vacuum dryers, high-efficiency pulverizers, double cone blenders, etc.
The packing specification is 25 KG per drum, with an annual production capacity of 180 tons.
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Levoamlodipine Besylate

Levoamlodipine Besylate

Modelo: CAS No.: 103129-82-4
Parâmetros: Molecular formula: C₂₀H₂₅ClN₂O₅·C₆H₆O₃
SAssay: 98.0%~102.0% on dried basis
Storage: Protected from light, sealed, cool & dry place
Specification: Complies with USP/EPGMP compliant
Single impurity & total impurity under tight control

Felodipine

Felodipine

Modelo: CAS No.: 72509-76-3
Parâmetros: Molecular formula: C18H19Cl2NO4
Assay: 98.0%~101.0% on dried basis
Storage: Protected from light, sealed, cool & dry place
Specification: Complies with USP/EP/BP
GMP compliant

Propafenone Hydrochloride

Propafenone Hydrochloride

Modelo: CAS No.: 34183-22-7
Parâmetros: EINECS No.: 251-867-9;
Molecular formula: C21H28ClNO3;
Molecular weight: 377.9049;
Boiling point: 519.6°C;
Flash point: 268°C;
Vapor pressure: 1.27E-11 mmHg at 25°C.

Tamsulosin Hydrochloride

Tamsulosin Hydrochloride

Modelo: CAS NO:106463-17-6;80223-99-0
Parâmetros: CAS No.: 106463-17-6; 80223-99-0
Molecular formula: C₂₀H₂₉ClN₂O₅S
Molecular weight: 444.9727
Melting point: 228–230℃
Boiling point: 595.5℃ at 760 mmHg
Flash point: 313.9℃
Vapor pressure: 3.79E-14 mmHg at 25℃

Amlodipine Besylate

Amlodipine Besylate

Modelo: CAS NO.:111470-99-6
Parâmetros: Assay: 98.0%~102.0%
Standard: USP / EP
Impurity: Strictly controlled
Melting point: 197℃ ~ 201℃
Packing: 25kg per drum
MOQ: 1kg

Galeria da empresa

Certificações e prêmios

Certificate of GMP Compliance of a Manufacturer
Certificate of GMP Compliance of a Manufacturer
EDQM Certificate of Suitability
EDQM Certificate of Suitability
Notice of GMP Compliance Inspection for Pharmaceutical Products
Notice of GMP Compliance Inspection for Pharmaceutical Products
Certificate of Suitability (CEP)
Certificate of Suitability (CEP)
Notice of GMP Compliance Inspection for Pharmaceutical Products
Notice of GMP Compliance Inspection for Pharmaceutical Products
Written confirmation for active substances exported to EU
Written confirmation for active substances exported to EU

Histórias de sucesso

Global cardiovascular pharma supply chain partner

Global cardiovascular pharma supply chain partner

Batch quality consistently meets EP requirements, stable impurity profile, passed supplier quality assessment, support commercial formulation production.
CEP dossier available, full batch traceability, flexible delivery schedule, audit-ready quality system

Localização: FR 📦 Quantity: 800–1000 kg per year

Vídeos da empresa e produtos

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Demonstração do produto - Kestrel K-1

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Showcase de inovação tecnológica

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Depoimentos de clientes e histórias de sucesso

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