01 1Tomita Pharmaceutical Co., Ltd.
01 1Japanese Pharmacopoeia Sodium Acetate Hydrate
01 1Japan
Japanese Pharmacopoeia Sodium Acetate Hydrate
Registration Number : 305MF10045
Registrant's Address : Tokushima Prefecture Naruto City Setocho Myojin Maruyama 85-1
Initial Date of Registration : 2023-04-05
Latest Date of Registration : 2023-04-05
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PharmaCompass offers a list of Sodium Acetate 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 Sodium Acetate manufacturer or Sodium Acetate supplier for your needs.
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PharmaCompass also assists you with knowing the Sodium Acetate API Price utilized in the formulation of products. Sodium Acetate API Price is not always fixed or binding as the Sodium Acetate Price is obtained through a variety of data sources. The Sodium Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KABIVEN IN PLASTIC CONTAINER-5 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KABIVEN IN PLASTIC CONTAINER-5, including repackagers and relabelers. The FDA regulates KABIVEN IN PLASTIC CONTAINER-5 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KABIVEN IN PLASTIC CONTAINER-5 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 KABIVEN IN PLASTIC CONTAINER-5 supplier is an individual or a company that provides KABIVEN IN PLASTIC CONTAINER-5 active pharmaceutical ingredient (API) or KABIVEN IN PLASTIC CONTAINER-5 finished formulations upon request. The KABIVEN IN PLASTIC CONTAINER-5 suppliers may include KABIVEN IN PLASTIC CONTAINER-5 API manufacturers, exporters, distributors and traders.
click here to find a list of KABIVEN IN PLASTIC CONTAINER-5 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 KABIVEN IN PLASTIC CONTAINER-5 Drug Master File in Japan (KABIVEN IN PLASTIC CONTAINER-5 JDMF) empowers KABIVEN IN PLASTIC CONTAINER-5 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 KABIVEN IN PLASTIC CONTAINER-5 JDMF during the approval evaluation for pharmaceutical products. At the time of KABIVEN IN PLASTIC CONTAINER-5 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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