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, and more, enabling you to easily find the right Acrylic Acid manufacturer or Acrylic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Acrylic Acid manufacturer or Acrylic Acid supplier.
A Carbomer 1342 (NF) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Carbomer 1342 (NF), including repackagers and relabelers. The FDA regulates Carbomer 1342 (NF) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Carbomer 1342 (NF) 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 Carbomer 1342 (NF) supplier is an individual or a company that provides Carbomer 1342 (NF) active pharmaceutical ingredient (API) or Carbomer 1342 (NF) finished formulations upon request. The Carbomer 1342 (NF) suppliers may include Carbomer 1342 (NF) API manufacturers, exporters, distributors and traders.
click here to find a list of Carbomer 1342 (NF) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Carbomer 1342 (NF) Drug Master File in Japan (Carbomer 1342 (NF) JDMF) empowers Carbomer 1342 (NF) 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 Carbomer 1342 (NF) JDMF during the approval evaluation for pharmaceutical products. At the time of Carbomer 1342 (NF) 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 Carbomer 1342 (NF) suppliers with JDMF on PharmaCompass.
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