With Fermion, start the journey of your innovative API.
01 1FERMION OY Espoo FI
02 1TEVA PHARMACEUTICAL INDUSTRIES LTD Tel Aviv - Jaffa IL
03 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1AUROBINDO PHARMA LIMITED Hyderabad IN
06 1CADILA PHARMACEUTICALS LIMITED Ankleshwar IN
07 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
08 1ESTEVE QUIMICA S.A. Barcelona ES
09 1Eli Lilly SA County Cork IE
10 1Erregierre S.p.A. San Paolo D'Argon IT
11 1GEDEON RICHTER PLC Budapest HU
12 1Lilly del Caribe, Inc - PR01 Carolina PR
13 2OLON S.P.A. Rodano IT
14 1Ranbaxy Laboratories Limited Gurgaon IN
15 2SIEGFRIED LTD. Zofingen CH
With Fermion, start the journey of your innovative API.
Certificate Number : R1-CEP 2009-354 - Rev 02
Status : Valid
Issue Date : 2020-12-21
Type : Chemical
Substance Number : 1104
TAPI offers customized CDMO Solutions for API development and manufacturing services.
Certificate Number : R1-CEP 1997-042 - Rev 11
Status : Valid
Issue Date : 2023-06-22
Type : Chemical
Substance Number : 1104
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 12 companies offering Fluoxetine Hydrochloride
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