Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1AARTI PHARMALABS LIMITED
01 1Korea United Pharmaceutical Co., Ltd.
01 1Mercaptopurine
01 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...
A Purinethol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Purinethol, including repackagers and relabelers. The FDA regulates Purinethol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Purinethol API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Purinethol supplier is an individual or a company that provides Purinethol active pharmaceutical ingredient (API) or Purinethol finished formulations upon request. The Purinethol suppliers may include Purinethol API manufacturers, exporters, distributors and traders.
click here to find a list of Purinethol 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 Purinethol Drug Master File in Korea (Purinethol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Purinethol. The MFDS reviews the Purinethol KDMF as part of the drug registration process and uses the information provided in the Purinethol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Purinethol 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 Purinethol API can apply through the Korea Drug Master File (KDMF).
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