Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1Wavelength Enterprises Ltd
02 1Dr. Reddy's Laboratories Ltd.
03 1Daito Co., Ltd.
04 1Permakem Asia Co., Ltd.
05 1SperaNexus Inc.
01 1CETIRIZINE DIHYDROCHLORIDE EP
02 3Cetirizine hydrochloride
03 1Japan Bureau Cetirizine Hydrochloride (for manufacturing only)
01 1France
02 1India
03 3Japan
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10400
Registrant's Address : Offer Park, Building C, 4th floor, 94 Shlomo Shmeltzer Road, POB 3158, Petah Tikva 49...
Initial Date of Registration : 2006-04-14
Latest Date of Registration : 2018-10-01
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 218MF10306
Registrant's Address : 8-2-337, Road No. 3,Banjara Hills,Hyderabad 500 034,TELANGANA,INDIA
Initial Date of Registration : 2006-04-20
Latest Date of Registration : 2006-12-18
JP Cetirizine Hydrochloride (For manufacturing only)
Registration Number : 220MF10084
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2008-03-18
Latest Date of Registration : 2008-03-18
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
A Cetirizine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cetirizine Hydrochloride, including repackagers and relabelers. The FDA regulates Cetirizine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cetirizine Hydrochloride 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 Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cetirizine Hydrochloride supplier is an individual or a company that provides Cetirizine Hydrochloride active pharmaceutical ingredient (API) or Cetirizine Hydrochloride finished formulations upon request. The Cetirizine Hydrochloride suppliers may include Cetirizine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cetirizine Hydrochloride 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 Cetirizine Hydrochloride Drug Master File in Japan (Cetirizine Hydrochloride JDMF) empowers Cetirizine Hydrochloride 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 Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Cetirizine Hydrochloride 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 Hydrochloride suppliers with JDMF on PharmaCompass.
We have 5 companies offering Cetirizine Hydrochloride
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