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01 1Virupaksha Organics Limited
02 1Virupaksha Organics Limited
03 1EUROAPI Germany GmbH
04 1Dr. Reddy's Laboratories Ltd.
05 1Amino Chemicals Ltd.
06 1Daito Co., Ltd.
07 1Dipharma Francis S. r. l.
08 2KOLON LIFE SCIENCE, INC.
09 1Organic Synthesis Chemicals Co., Ltd.
10 2Osaka Synthetic Organic Chemistry Laboratory Co., Ltd.
11 1Pharmacostech CO. ,LTD
12 1Sumitomo Chemical Co., Ltd.
13 1Synthimed Labs Private Limited
01 3Fexofenadine Hydrochloride
02 1Fexofenadine Hydrochloride (C)
03 7Fexofenadine hydrochloride
04 2Japanese Pharmacopoeia fexofenadine hydrochloride
05 2Japanese Pharmacopoeia fexofenadine hydrochloride salt production dedicated
01 1France
02 4India
03 1Italy
04 5Japan
05 1Malta
06 3South Korea
Japanese Pharmacopoeia Fexofenadine Hydrochloride
Registration Number : 229MF10083
Registrant's Address : B-4,IDA,Gandhinagar,Hyderabad-500037,Telangana,INDIA
Initial Date of Registration : 2017-04-11
Latest Date of Registration : 2017-04-11
Registration Number : 302MF10017
Registrant's Address : Brueningstrasse 50, 65926 Frankfurt am Main, Germany
Initial Date of Registration : 2020-01-31
Latest Date of Registration : 2020-01-31
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 302MF10124
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2020-10-05
Latest Date of Registration : 2020-10-05
Registration Number : 226MF10224
Registrant's Address : Survey No. 10, Gaddapotharam Village, Jinnaram Mandal, Medak Dist. -502 319, Telangan...
Initial Date of Registration : 2014-12-08
Latest Date of Registration : 2014-12-08
Registration Number : 222MF10270
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2010-12-10
Latest Date of Registration : 2022-09-29
Registration Number : 228MF10070
Registrant's Address : Via Bissone, 5, 20021-Baranzate, Milano, Italy
Initial Date of Registration : 2016-03-02
Latest Date of Registration : 2021-11-17
Registration Number : 226MF10024
Registrant's Address : Village-Bhagwanpur, Barwala Road, Derabassi-140 507 District-S. A. S. Nagar (Mohali)P...
Initial Date of Registration : 2014-01-21
Latest Date of Registration : 2018-08-08
Fexofenadine hydrochloride (C)
Registration Number : 302MF10093
Registrant's Address : 110, MAGOKDONG-RO, GANGSEO-GU, SEOUL, KOREA
Initial Date of Registration : 2020-08-05
Latest Date of Registration : 2020-08-05
Japanese Pharmacopoeia Fexofenadine Hydrochloride For manufacturing only
Registration Number : 230MF10064
Registrant's Address : 1-1-2 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2018-05-08
Latest Date of Registration : 2018-05-08
Japanese Pharmacopoeia Fexofenadine Hydrochloride
Registration Number : 223MF10088
Registrant's Address : 2-7-1 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2011-06-27
Latest Date of Registration : 2021-08-16
A Fexofenadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fexofenadine Hydrochloride, including repackagers and relabelers. The FDA regulates Fexofenadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fexofenadine 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 Fexofenadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fexofenadine Hydrochloride supplier is an individual or a company that provides Fexofenadine Hydrochloride active pharmaceutical ingredient (API) or Fexofenadine Hydrochloride finished formulations upon request. The Fexofenadine Hydrochloride suppliers may include Fexofenadine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fexofenadine 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 Fexofenadine Hydrochloride Drug Master File in Japan (Fexofenadine Hydrochloride JDMF) empowers Fexofenadine 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 Fexofenadine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Fexofenadine 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 Fexofenadine Hydrochloride suppliers with JDMF on PharmaCompass.
We have 12 companies offering Fexofenadine Hydrochloride
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