01 2Henkel Corporation
02 1Henkel Corporation
01 1DURO-TAK 387-2051 / 87-2051
02 1DURO-TAK 387-2054 / 87-2054
03 1DURO-TAK 387-2353 / 87-2353
01 3U.S.A
Registration Number : 221MF20003
Registrant's Address : 10 Finderne Avenue Bridgewater, NJ 08807, USA
Initial Date of Registration : 2009-10-08
Latest Date of Registration : 2015-10-28
Registration Number : 220MF20003
Registrant's Address : 10 Finderne Avenue Bridgewater, NJ 08807, USA
Initial Date of Registration : 2008-11-04
Latest Date of Registration : 2015-10-28
Registration Number : 220MF20002
Registrant's Address : 10 Finderne Avenue Bridgewater, NJ 08807, USA
Initial Date of Registration : 2008-11-04
Latest Date of Registration : 2015-10-28
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PharmaCompass offers a list of Acrylic Acid 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 Acrylic Acid manufacturer or Acrylic Acid supplier for your needs.
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PharmaCompass also assists you with knowing the Acrylic Acid API Price utilized in the formulation of products. Acrylic Acid API Price is not always fixed or binding as the Acrylic Acid Price is obtained through a variety of data sources. The Acrylic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 9003-01-4 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 9003-01-4, including repackagers and relabelers. The FDA regulates 9003-01-4 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 9003-01-4 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A 9003-01-4 supplier is an individual or a company that provides 9003-01-4 active pharmaceutical ingredient (API) or 9003-01-4 finished formulations upon request. The 9003-01-4 suppliers may include 9003-01-4 API manufacturers, exporters, distributors and traders.
click here to find a list of 9003-01-4 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 9003-01-4 Drug Master File in Japan (9003-01-4 JDMF) empowers 9003-01-4 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 9003-01-4 JDMF during the approval evaluation for pharmaceutical products. At the time of 9003-01-4 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 9003-01-4 suppliers with JDMF on PharmaCompass.
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