01 2BASILDON CHEMICAL CO. LIMITED
02 1DDP Specialty Electronic Materials US 9, LLC
01 1AFC2-2671 (Simeticone)
02 1BC Simeticone Antifoam PD30S (Simeticone Emulsion)
03 1LiveoTM Q7-2243 LVA, Simeticone USP
01 1U.S.A
02 2United Kingdom
BC Simethicone Antifoam PD30S (Simethicone Emulsion)
Registration Number : 302MF20002
Registrant's Address : Kimber Road, Abingdon, Oxon, OX14 1RZ, United Kingdom
Initial Date of Registration : 2020-08-18
Latest Date of Registration : 2022-10-19
Registration Number : 302MF20001
Registrant's Address : Kimber Road, Abingdon, Oxon, OX14 1RZ, United Kingdom
Initial Date of Registration : 2020-08-05
Latest Date of Registration : 2020-08-05
LiveoTM Q7-2243 LVA, Simethicone USP
Registration Number : 303MF10114
Registrant's Address : 974 Center Road, Wilmington, DE 19805, USA
Initial Date of Registration : 2021-07-16
Latest Date of Registration : 2021-07-16
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PharmaCompass offers a list of Simethicone 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 Simethicone manufacturer or Simethicone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Simethicone manufacturer or Simethicone supplier.
PharmaCompass also assists you with knowing the Simethicone API Price utilized in the formulation of products. Simethicone API Price is not always fixed or binding as the Simethicone Price is obtained through a variety of data sources. The Simethicone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Wydrate Plus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Wydrate Plus, including repackagers and relabelers. The FDA regulates Wydrate Plus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Wydrate Plus 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 Wydrate Plus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Wydrate Plus supplier is an individual or a company that provides Wydrate Plus active pharmaceutical ingredient (API) or Wydrate Plus finished formulations upon request. The Wydrate Plus suppliers may include Wydrate Plus API manufacturers, exporters, distributors and traders.
click here to find a list of Wydrate Plus 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 Wydrate Plus Drug Master File in Japan (Wydrate Plus JDMF) empowers Wydrate Plus 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 Wydrate Plus JDMF during the approval evaluation for pharmaceutical products. At the time of Wydrate Plus 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 Wydrate Plus suppliers with JDMF on PharmaCompass.
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