Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI PHARMALABS LIMITED
02 1Zhejiang Cheng Yi Pharmaceutical Co., Ltd.
01 1Korea United Pharmaceutical Co., Ltd.
02 1Pharmapia Co., Ltd.
01 2Mercaptopurine
01 1China
02 1India
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Registrant Name : Korea United Pharmaceutical Co., Ltd.
Registration Date : 2022-05-27
Registration Number : 20220527-209-J-1309
Manufacturer Name : AARTI PHARMALABS LIMITED
Manufacturer Address : PLOT NO. E-50, 50/1 AND 59/1, UNIT-IV, MIDC, TARAPUR, TALUKA & DISTRICT - PALGHAR 401...
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2025-02-24
Registration Number : 20250224-209-J-1771
Manufacturer Name : Zhejiang Cheng Yi Pharmaceut...
Manufacturer Address : 118 Hua Gong Road, Dongtou District, Wenzhou, Zhejiang Province 325700, China
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PharmaCompass offers a list of Mercaptopurine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Mercaptopurine manufacturer or Mercaptopurine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Mercaptopurine manufacturer or Mercaptopurine supplier.
PharmaCompass also assists you with knowing the Mercaptopurine API Price utilized in the formulation of products. Mercaptopurine API Price is not always fixed or binding as the Mercaptopurine Price is obtained through a variety of data sources. The Mercaptopurine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PURIXAN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PURIXAN, including repackagers and relabelers. The FDA regulates PURIXAN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PURIXAN API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of PURIXAN manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PURIXAN supplier is an individual or a company that provides PURIXAN active pharmaceutical ingredient (API) or PURIXAN finished formulations upon request. The PURIXAN suppliers may include PURIXAN API manufacturers, exporters, distributors and traders.
click here to find a list of PURIXAN suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a PURIXAN Drug Master File in Korea (PURIXAN KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of PURIXAN. The MFDS reviews the PURIXAN KDMF as part of the drug registration process and uses the information provided in the PURIXAN KDMF to evaluate the safety and efficacy of the drug.
After submitting a PURIXAN KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their PURIXAN API can apply through the Korea Drug Master File (KDMF).
click here to find a list of PURIXAN suppliers with KDMF on PharmaCompass.
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