01 1Apitoria Pharma Private Limited
02 2Aurobindo Pharma Limited
03 1Fresenius Kabi iPSUM S. r. l.
04 1Jiangxi Fushine Pharmaceutical Co. , Ltd.
05 1Otsuka Chemical Co., Ltd.
06 1Shandong Anshun Pharmaceutical Co. , Ltd.
07 2Shandong Anxin Pharmaceutical Co. , Ltd.
08 1THE UNITED LABORATORIES (INNER MONGOLIA) CO. , LTD.
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PharmaCompass offers a list of Tazobactam Sodium 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 Tazobactam Sodium manufacturer or Tazobactam Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Tazobactam Sodium API Price utilized in the formulation of products. Tazobactam Sodium API Price is not always fixed or binding as the Tazobactam Sodium Price is obtained through a variety of data sources. The Tazobactam Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ZOSYN IN PLASTIC CONTAINER-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ZOSYN IN PLASTIC CONTAINER-1, including repackagers and relabelers. The FDA regulates ZOSYN IN PLASTIC CONTAINER-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ZOSYN IN PLASTIC CONTAINER-1 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 ZOSYN IN PLASTIC CONTAINER-1 supplier is an individual or a company that provides ZOSYN IN PLASTIC CONTAINER-1 active pharmaceutical ingredient (API) or ZOSYN IN PLASTIC CONTAINER-1 finished formulations upon request. The ZOSYN IN PLASTIC CONTAINER-1 suppliers may include ZOSYN IN PLASTIC CONTAINER-1 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 ZOSYN IN PLASTIC CONTAINER-1 Drug Master File in Japan (ZOSYN IN PLASTIC CONTAINER-1 JDMF) empowers ZOSYN IN PLASTIC CONTAINER-1 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 ZOSYN IN PLASTIC CONTAINER-1 JDMF during the approval evaluation for pharmaceutical products. At the time of ZOSYN IN PLASTIC CONTAINER-1 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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