01 1Zhejiang Huahai Pharmaceutical Co. , Ltd.
01 1Nevirapine
01 1China
Registration Number : 227MF10149
Registrant's Address : Xunqiao, Linhai, Zhejiang 317024, China
Initial Date of Registration : 2015-05-26
Latest Date of Registration : 2021-03-17
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PharmaCompass offers a list of Nevirapine 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 Nevirapine manufacturer or Nevirapine supplier for your needs.
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A NEVIRAPINE TABLETS FOR ORAL SUSPENSION manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NEVIRAPINE TABLETS FOR ORAL SUSPENSION, including repackagers and relabelers. The FDA regulates NEVIRAPINE TABLETS FOR ORAL SUSPENSION manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NEVIRAPINE TABLETS FOR ORAL SUSPENSION 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 NEVIRAPINE TABLETS FOR ORAL SUSPENSION supplier is an individual or a company that provides NEVIRAPINE TABLETS FOR ORAL SUSPENSION active pharmaceutical ingredient (API) or NEVIRAPINE TABLETS FOR ORAL SUSPENSION finished formulations upon request. The NEVIRAPINE TABLETS FOR ORAL SUSPENSION suppliers may include NEVIRAPINE TABLETS FOR ORAL SUSPENSION API manufacturers, exporters, distributors and traders.
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The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The NEVIRAPINE TABLETS FOR ORAL SUSPENSION Drug Master File in Japan (NEVIRAPINE TABLETS FOR ORAL SUSPENSION JDMF) empowers NEVIRAPINE TABLETS FOR ORAL SUSPENSION API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the NEVIRAPINE TABLETS FOR ORAL SUSPENSION JDMF during the approval evaluation for pharmaceutical products. At the time of NEVIRAPINE TABLETS FOR ORAL SUSPENSION JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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