01 1Dr. Paul Lohmann GmbH & Co. KGaA
02 1Komatsuya Co., Ltd.
03 1Satsuma Chemical 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 Standard 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 Standard Potassium Citrate
Registration Number : 220MF10118
Registrant's Address : 1451 Kaseda Kawabata, Minamisatsuma City, Kagoshima 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 Litocit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Litocit, including repackagers and relabelers. The FDA regulates Litocit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Litocit 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 Litocit supplier is an individual or a company that provides Litocit active pharmaceutical ingredient (API) or Litocit finished formulations upon request. The Litocit suppliers may include Litocit 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 Litocit Drug Master File in Japan (Litocit JDMF) empowers Litocit 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 Litocit JDMF during the approval evaluation for pharmaceutical products. At the time of Litocit 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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