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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
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01 9Fexofenadine hydrochloride
02 1Fexofenadine hydrochloride, Form-I
03 1Fexofenadine hydrochloride, Process-II
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01 1France
02 10India
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01 9Valid
02 2Withdrawn by Holder
Certificate Number : CEP 2009-160 - Rev 04
Status : Valid
Issue Date : 2024-07-17
Type : Chemical
Substance Number : 2280
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.
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
Certificate Number : CEP 2018-101 - Rev 01
Status : Valid
Issue Date : 2024-02-23
Type : Chemical
Substance Number : 2280
Certificate Number : CEP 2012-278 - Rev 03
Status : Valid
Issue Date : 2024-03-12
Type : Chemical
Substance Number : 2280
Certificate Number : R1-CEP 2015-256 - Rev 00
Status : Valid
Issue Date : 2021-09-16
Type : Chemical
Substance Number : 2280
Certificate Number : R1-CEP 2008-247 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2015-06-09
Type : Chemical
Substance Number : 2280
Fexofenadine Hydrochloride, Process-II
Certificate Number : CEP 2022-420 - Rev 01
Status : Valid
Issue Date : 2024-08-01
Type : Chemical
Substance Number : 2280
Certificate Number : CEP 2008-226 - Rev 03
Status : Valid
Issue Date : 2024-08-05
Type : Chemical
Substance Number : 2280
Certificate Number : CEP 2015-234 - Rev 02
Status : Valid
Issue Date : 2024-06-12
Type : Chemical
Substance Number : 2280
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PharmaCompass offers a list of Fexofenadine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Fexofenadine Hydrochloride manufacturer or Fexofenadine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fexofenadine Hydrochloride manufacturer or Fexofenadine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Fexofenadine Hydrochloride API Price utilized in the formulation of products. Fexofenadine Hydrochloride API Price is not always fixed or binding as the Fexofenadine Hydrochloride Price is obtained through a variety of data sources. The Fexofenadine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Allegra Allergy manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Allegra Allergy, including repackagers and relabelers. The FDA regulates Allegra Allergy manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Allegra Allergy 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 Allegra Allergy manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Allegra Allergy supplier is an individual or a company that provides Allegra Allergy active pharmaceutical ingredient (API) or Allegra Allergy finished formulations upon request. The Allegra Allergy suppliers may include Allegra Allergy API manufacturers, exporters, distributors and traders.
click here to find a list of Allegra Allergy suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Allegra Allergy CEP of the European Pharmacopoeia monograph is often referred to as a Allegra Allergy Certificate of Suitability (COS). The purpose of a Allegra Allergy CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Allegra Allergy EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Allegra Allergy to their clients by showing that a Allegra Allergy CEP has been issued for it. The manufacturer submits a Allegra Allergy CEP (COS) as part of the market authorization procedure, and it takes on the role of a Allegra Allergy CEP holder for the record. Additionally, the data presented in the Allegra Allergy CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Allegra Allergy DMF.
A Allegra Allergy CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Allegra Allergy 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 Allegra Allergy suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Allegra Allergy
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