01 1Specialty Products US, LLC
01 1Poly (ethylene oxide)
01 1U.S.A
Registration Number : 218MF20001
Registrant's Address : 2211 H. H. Dow Way, Midland MI 48674, United States
Initial Date of Registration : 2006-02-23
Latest Date of Registration : 2023-06-21
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PharmaCompass offers a list of Lauromacrogol 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 Lauromacrogol manufacturer or Lauromacrogol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lauromacrogol manufacturer or Lauromacrogol supplier.
PharmaCompass also assists you with knowing the Lauromacrogol API Price utilized in the formulation of products. Lauromacrogol API Price is not always fixed or binding as the Lauromacrogol Price is obtained through a variety of data sources. The Lauromacrogol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A PEG-400 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PEG-400, including repackagers and relabelers. The FDA regulates PEG-400 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PEG-400 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 PEG-400 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A PEG-400 supplier is an individual or a company that provides PEG-400 active pharmaceutical ingredient (API) or PEG-400 finished formulations upon request. The PEG-400 suppliers may include PEG-400 API manufacturers, exporters, distributors and traders.
click here to find a list of PEG-400 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 PEG-400 Drug Master File in Japan (PEG-400 JDMF) empowers PEG-400 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 PEG-400 JDMF during the approval evaluation for pharmaceutical products. At the time of PEG-400 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 PEG-400 suppliers with JDMF on PharmaCompass.
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