01 1Dr. Paul Lohmann GmbH & Co. KGaA
02 1Komatsuya Co., Ltd.
03 1Showa Kako Co., Ltd.
01 2Japan Pharmaceutical Codex potassium citrate
02 1Potassium citrate
01 1Germany
02 2Japan
Registration Number : 221MF10109
Registrant's Address : Hauptstrasse 2 D-31860 Emmerthal Germany
Initial Date of Registration : 2009-06-02
Latest Date of Registration : 2009-06-02
Japanese Pharmacopoeia Non-Drug Standards Potassium Citrate
Registration Number : 219MF10180
Registrant's Address : Matsuura Sakaisuji Honmachi Building, 1-9-28 Kyutarocho, Chuo-ku, Osaka City, Osaka P...
Initial Date of Registration : 2007-06-01
Latest Date of Registration : 2007-06-01
Japanese Pharmacopoeia Non-Drug Standards Potassium Citrate
Registration Number : 220MF10118
Registrant's Address : 18-23 Yoshinocho, Suita City, Osaka Prefecture
Initial Date of Registration : 2008-04-28
Latest Date of Registration : 2008-04-28
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PharmaCompass offers a list of Potassium Citrate 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 Potassium Citrate manufacturer or Potassium Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Citrate manufacturer or Potassium Citrate supplier.
PharmaCompass also assists you with knowing the Potassium Citrate API Price utilized in the formulation of products. Potassium Citrate API Price is not always fixed or binding as the Potassium Citrate Price is obtained through a variety of data sources. The Potassium Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Urocit K manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urocit K, including repackagers and relabelers. The FDA regulates Urocit K manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urocit K 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 Urocit K manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urocit K supplier is an individual or a company that provides Urocit K active pharmaceutical ingredient (API) or Urocit K finished formulations upon request. The Urocit K suppliers may include Urocit K API manufacturers, exporters, distributors and traders.
click here to find a list of Urocit K 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 Urocit K Drug Master File in Japan (Urocit K JDMF) empowers Urocit K 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 Urocit K JDMF during the approval evaluation for pharmaceutical products. At the time of Urocit K JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Urocit K suppliers with JDMF on PharmaCompass.
We have 3 companies offering Urocit K
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