河南普瑞制药有限公司

河南普瑞制药有限公司

河南普瑞制药有限公司

河南普瑞制药有限公司

Main Products:苯乙酸甲酯, 6-羟基托品酮, D-阿拉伯糖,
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China methyl formylphenylacetate - China Supplier

methyl formylphenylacetate

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China (2R)-2-(3-fluoro-4-phenyl-phenyl)propanoic acid - China Supplier

(2R)-2-(3-fluoro-4-phenyl-phenyl)propanoic acid

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China 1,3,5-Trimethoxybenzene - China Supplier

1,3,5-Trimethoxybenzene

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China sucrose octasulfate - aluminum complex - China Supplier

sucrose octasulfate - aluminum complex

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China Magnesium trisilicate - China Supplier

Magnesium trisilicate

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China Aminomethylbenzoic acid - China Supplier

Aminomethylbenzoic acid

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China Neostigmine methyl sulfate - China Supplier

Neostigmine methyl sulfate

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China Urapidil hydrochloride - China Supplier

Urapidil hydrochloride

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China Dobutamine HCL - China Supplier

Dobutamine HCL

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China Ethyl 4-hydroxy-2-methyl-1,1-dioxo-2H-1,2-benzothiazine-3-carboxylate - China Supplier

Ethyl 4-hydroxy-2-methyl-1,1-dioxo-2H-1,2-benzothiazine-3-carboxylate

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Company Profile

河南普瑞制药有限公司

    Henan Purui Pharmaceutical Co., Ltd., located in Xihua County, Henan Province, covers an area of over 20,000 square meters. It is a specialized manufacturer of anticholinergic active pharmaceutical ingredients (APIs) in China and an important export base, certified by the National GMP (Good Manufacturing Practice) standards.

    The company currently employs over 300 staff, including 72 professional and technical personnel (with intermediate and senior professional titles), and has fixed assets worth 40 million RMB. With strong technical capabilities, advanced production processes, and comprehensive testing instruments, the company strictly adheres to the "Good Manufacturing Practice for Pharmaceutical Products" in organizing production. It has established long-term cooperative relationships with the School of Pharmacy of Zhengzhou University and the Zhengzhou University New Drug R&D Center. On November 1, 2009, the company successfully passed the GMP inspection by the National Medical Products Administration (certificate numbers KO105 and G0037). It specializes in the production of APIs such as Racemic Anisodamine (National Drug Approval Number H19983090), Atropine Sulfate (National Drug Approval Number H20073819), Levofloxacin Hydrochloride, as well as various pharmaceutical intermediates including Tropine and Tropinol.

    The company adheres to the management principle of "Quality First, People-Oriented," embraces a corporate spirit of keeping pace with the times and forging ahead with determination, and builds the image of Purui Pharmaceutical professionals with integrity.


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