Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.

Reset all filters
01 1Wavelength Enterprises Ltd
02 1Permachem Asia Co., Ltd.
03 1Speranexus Co., Ltd.
Reset all filters
01 3Cetirizine hydrochloride
Reset all filters
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

63
PharmaCompass offers a list of Cetirizine Dihydrochloride 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 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.
A Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard, including repackagers and relabelers. The FDA regulates Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard supplier is an individual or a company that provides Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard active pharmaceutical ingredient (API) or Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard finished formulations upon request. The Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers may include Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard API manufacturers, exporters, distributors and traders.
click here to find a list of Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard Drug Master File in Japan (Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard JDMF) empowers Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard JDMF during the approval evaluation for pharmaceutical products. At the time of Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard 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 Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard suppliers with JDMF on PharmaCompass.
We have 3 companies offering Cetirizine dihydrochloride, United States Pharmacopeia (USP) Reference Standard
Get in contact with the supplier of your choice: