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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
With Virupaksha, you get a quality product with on-time delivery.
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
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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
With Virupaksha, you get a quality product with on-time delivery.
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
A Fexofenadine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fexofenadine, including repackagers and relabelers. The FDA regulates Fexofenadine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fexofenadine 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fexofenadine supplier is an individual or a company that provides Fexofenadine active pharmaceutical ingredient (API) or Fexofenadine finished formulations upon request. The Fexofenadine suppliers may include Fexofenadine API manufacturers, exporters, distributors and traders.
click here to find a list of Fexofenadine 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 Drug Master File in Japan (Fexofenadine JDMF) empowers Fexofenadine 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Fexofenadine 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 suppliers with JDMF on PharmaCompass.
We have 12 companies offering Fexofenadine
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