01 1Clariant Products (Deutschland) GmbH
02 1Sanyo Chemical Industries, Ltd.
01 1Macrogol 4000 (Hunmatsu)
02 1Polyglykol 3350
01 1Japan
02 1Switzerland
Registration Number : 229MF10099
Registrant's Address : Bru(¨)ningstraβe 50, D-65926 Frankfurt/Main
Initial Date of Registration : 2017-05-29
Latest Date of Registration : 2025-07-09
Registration Number : 304MF10097
Registrant's Address : 11-1 Hitotsubashinomotocho, Higashiyama-ku, Kyoto City, Kyoto Prefecture
Initial Date of Registration : 2022-07-06
Latest Date of Registration : 2023-04-19
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PharmaCompass offers a list of Macrogol 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 Macrogol manufacturer or Macrogol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Macrogol manufacturer or Macrogol supplier.
PharmaCompass also assists you with knowing the Macrogol API Price utilized in the formulation of products. Macrogol API Price is not always fixed or binding as the Macrogol Price is obtained through a variety of data sources. The Macrogol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lutrol E (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lutrol E (TN), including repackagers and relabelers. The FDA regulates Lutrol E (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lutrol E (TN) 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 Lutrol E (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lutrol E (TN) supplier is an individual or a company that provides Lutrol E (TN) active pharmaceutical ingredient (API) or Lutrol E (TN) finished formulations upon request. The Lutrol E (TN) suppliers may include Lutrol E (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Lutrol E (TN) 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 Lutrol E (TN) Drug Master File in Japan (Lutrol E (TN) JDMF) empowers Lutrol E (TN) 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 Lutrol E (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Lutrol E (TN) 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 Lutrol E (TN) suppliers with JDMF on PharmaCompass.
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