With Virupaksha, you get a quality product with on-time delivery.
01 1VIRUPAKSHA ORGANICS LIMITED Hyderabad IN
02 1EUROAPI GERMANY GmbH Frankfurt am Main DE
03 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
04 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1CIPLA LIMITED Mumbai IN
06 1HETERO DRUGS LIMITED Hyderabad IN
07 1MOREPEN LABORATORIES LIMITED New Delhi IN
08 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
09 2SYNTHIMED LABS PRIVATE LIMITED Derabassi IN
10 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
With Virupaksha, you get a quality product with on-time delivery.
Certificate Number : CEP 2009-160 - Rev 04
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 2280
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
Certificate Number : R1-CEP 2009-297 - Rev 03
Status : Valid
Issue Date : 2021-12-09
Type : Chemical
Substance Number : 2280
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Fexofenadine Hydrochloride, Form-I
Certificate Number : R0-CEP 2021-067 - Rev 00
Status : Valid
Issue Date : 2023-07-06
Type : Chemical
Substance Number : 2280
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.
A Fexofenadine CEP of the European Pharmacopoeia monograph is often referred to as a Fexofenadine Certificate of Suitability (COS). The purpose of a Fexofenadine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fexofenadine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fexofenadine to their clients by showing that a Fexofenadine CEP has been issued for it. The manufacturer submits a Fexofenadine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fexofenadine CEP holder for the record. Additionally, the data presented in the Fexofenadine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fexofenadine DMF.
A Fexofenadine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fexofenadine CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Fexofenadine suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Fexofenadine
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