Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
01 1Wavelength Enterprises Ltd
02 1Permachem Asia Co., Ltd.
03 1Speranexus Co., Ltd.
01 3Cetirizine hydrochloride
01 1France
02 2Japan
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Registration Number : 218MF10400
Registrant's Address : Ofer Park, Building E, 5th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva 497...
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2018-10-01
Registration Number : 218MF10273
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-02-23
Latest Date of Registration : 2007-01-22
Registration Number : 218MF10005
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2006-01-12
Latest Date of Registration : 2006-12-27
61
PharmaCompass offers a list of Cetirizine Dihydrochloride 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 Cetirizine Dihydrochloride manufacturer or Cetirizine Dihydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cetirizine Dihydrochloride manufacturer or Cetirizine Dihydrochloride supplier.
PharmaCompass also assists you with knowing the Cetirizine Dihydrochloride API Price utilized in the formulation of products. Cetirizine Dihydrochloride API Price is not always fixed or binding as the Cetirizine Dihydrochloride Price is obtained through a variety of data sources. The Cetirizine Dihydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A D00664 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of D00664, including repackagers and relabelers. The FDA regulates D00664 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. D00664 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 D00664 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A D00664 supplier is an individual or a company that provides D00664 active pharmaceutical ingredient (API) or D00664 finished formulations upon request. The D00664 suppliers may include D00664 API manufacturers, exporters, distributors and traders.
click here to find a list of D00664 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 D00664 Drug Master File in Japan (D00664 JDMF) empowers D00664 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 D00664 JDMF during the approval evaluation for pharmaceutical products. At the time of D00664 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 D00664 suppliers with JDMF on PharmaCompass.
We have 3 companies offering D00664
Get in contact with the supplier of your choice:
