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01 1FERMION OY Espoo FI
02 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1AUROBINDO PHARMA LIMITED Hyderabad IN
05 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
06 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
07 1ESTEVE QUIMICA S.A. Barcelona ES
08 1Eli Lilly SA County Cork IE
09 1Erregierre S.p.A. San Paolo D'Argon IT
10 1GEDEON RICHTER PLC Budapest HU
11 1Lilly del Caribe, Inc - PR01 Carolina PR
12 2OLON S.P.A. Rodano IT
13 1Ranbaxy Laboratories Limited Gurgaon IN
14 2SIEGFRIED LTD. Zofingen CH
15 1TAPI NL B.V. Amsterdam NL
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01 15Fluoxetine hydrochloride
02 1Fluoxetine hydrochloride, Code 292786
03 2Fluoxetine hydrochloride, Process II
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01 1Finland
02 1Hungary
03 7India
04 3Italy
05 1Spain
06 2Switzerland
07 2U.S.A
08 1Blank
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01 12Valid
02 6Withdrawn by Holder
Certificate Number : R1-CEP 2009-354 - Rev 02
Status : Valid
Issue Date : 2020-12-21
Type : Chemical
Substance Number : 1104
Certificate Number : R1-CEP 2013-199 - Rev 02
Status : Valid
Issue Date : 2023-03-15
Type : Chemical
Substance Number : 1104
Fluoxetine Hydrochloride, Process II
Certificate Number : CEP 2019-226 - Rev 04
Status : Valid
Issue Date : 2025-02-26
Type : Chemical
Substance Number : 1104
Certificate Number : R1-CEP 2004-207 - Rev 06
Status : Valid
Issue Date : 2022-03-07
Type : Chemical
Substance Number : 1104
Certificate Number : CEP 1999-071 - Rev 06
Status : Valid
Issue Date : 2024-05-27
Type : Chemical
Substance Number : 1104
Certificate Number : CEP 2007-033 - Rev 06
Status : Valid
Issue Date : 2023-12-15
Type : Chemical
Substance Number : 1104
Certificate Number : CEP 2003-231 - Rev 05
Status : Valid
Issue Date : 2024-02-19
Type : Chemical
Substance Number : 1104
Fluoxetine Hydrochloride, Code 292786
Certificate Number : R1-CEP 2008-178 - Rev 01
Status : Valid
Issue Date : 2020-12-01
Type : Chemical
Substance Number : 1104
Certificate Number : R1-CEP 1999-171 - Rev 06
Status : Valid
Issue Date : 2018-06-25
Type : Chemical
Substance Number : 1104
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Certificate Number : CEP 1997-042 - Rev 12
Status : Valid
Issue Date : 2025-03-12
Type : Chemical
Substance Number : 1104
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PharmaCompass offers a list of Fluoxetine 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 Fluoxetine manufacturer or Fluoxetine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluoxetine manufacturer or Fluoxetine supplier.
PharmaCompass also assists you with knowing the Fluoxetine API Price utilized in the formulation of products. Fluoxetine API Price is not always fixed or binding as the Fluoxetine Price is obtained through a variety of data sources. The Fluoxetine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fluoxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluoxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Fluoxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluoxetine 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 Fluoxetine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluoxetine Hydrochloride supplier is an individual or a company that provides Fluoxetine Hydrochloride active pharmaceutical ingredient (API) or Fluoxetine Hydrochloride finished formulations upon request. The Fluoxetine Hydrochloride suppliers may include Fluoxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fluoxetine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fluoxetine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Fluoxetine Hydrochloride Certificate of Suitability (COS). The purpose of a Fluoxetine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Fluoxetine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Fluoxetine Hydrochloride to their clients by showing that a Fluoxetine Hydrochloride CEP has been issued for it. The manufacturer submits a Fluoxetine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Fluoxetine Hydrochloride CEP holder for the record. Additionally, the data presented in the Fluoxetine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Fluoxetine Hydrochloride DMF.
A Fluoxetine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Fluoxetine Hydrochloride 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 Fluoxetine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 11 companies offering Fluoxetine Hydrochloride
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