01 2AESICA PHARMACEUTICALS LIMITED Cramlington GB
02 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
03 1CHEMI S.P.A. Patrica IT
04 1GEDEON RICHTER PLC Budapest HU
05 1IPCA Laboratories Limited Mumbai IN
06 1JUBILANT PHARMOVA LIMITED Nanjangud IN
07 1Medichem, S.A. Sant Joan Despí ES
08 2TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
09 1Wanbury Limited Vashi, Navi Mumbai IN
10 2ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
11 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
12 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
01 3Paroxetine hydrochloride
02 12Paroxetine hydrochloride hemihydrate
01 3China
02 1Hungary
03 7India
04 1Italy
05 1Spain
06 2United Kingdom
01 1Expired
02 12Valid
03 2Withdrawn by Holder
Paroxetine Hydrochloride Hemihydrate
Certificate Number : CEP 2006-206 - Rev 04
Status : Valid
Issue Date : 2023-12-13
Type : Chemical
Substance Number : 2018
Paroxetine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2011-188 - Rev 02
Status : Valid
Issue Date : 2020-06-19
Type : Chemical
Substance Number : 2018
Paroxetine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2014-095 - Rev 00
Status : Valid
Issue Date : 2021-01-11
Type : Chemical
Substance Number : 2018
Paroxetine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2009-204 - Rev 02
Status : Valid
Issue Date : 2022-08-23
Type : Chemical
Substance Number : 2018
Paroxetine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2011-200 - Rev 00
Status : Valid
Issue Date : 2018-03-05
Type : Chemical
Substance Number : 2018
Paroxetine Hydrochloride Hemihydrate
Certificate Number : CEP 2009-154 - Rev 03
Status : Valid
Issue Date : 2024-07-19
Type : Chemical
Substance Number : 2018
Certificate Number : CEP 2009-155 - Rev 04
Status : Valid
Issue Date : 2024-07-19
Type : Chemical
Substance Number : 2283
Paroxetine Hydrochloride Hemihydrate
Certificate Number : R1-CEP 2006-192 - Rev 01
Status : Valid
Issue Date : 2017-06-27
Type : Chemical
Substance Number : 2018
Certificate Number : R1-CEP 2006-002 - Rev 01
Status : Valid
Issue Date : 2014-01-06
Type : Chemical
Substance Number : 2283
Paroxetine Hydrochloride Hemihydrate
Certificate Number : CEP 2004-239 - Rev 07
Status : Valid
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 2018
73
PharmaCompass offers a list of Paroxetine 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 Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Paroxetine Hydrochloride API Price utilized in the formulation of products. Paroxetine Hydrochloride API Price is not always fixed or binding as the Paroxetine Hydrochloride Price is obtained through a variety of data sources. The Paroxetine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paxil CR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paxil CR, including repackagers and relabelers. The FDA regulates Paxil CR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paxil CR API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Paxil CR supplier is an individual or a company that provides Paxil CR active pharmaceutical ingredient (API) or Paxil CR finished formulations upon request. The Paxil CR suppliers may include Paxil CR API manufacturers, exporters, distributors and traders.
click here to find a list of Paxil CR suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Paxil CR CEP of the European Pharmacopoeia monograph is often referred to as a Paxil CR Certificate of Suitability (COS). The purpose of a Paxil CR CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Paxil CR EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Paxil CR to their clients by showing that a Paxil CR CEP has been issued for it. The manufacturer submits a Paxil CR CEP (COS) as part of the market authorization procedure, and it takes on the role of a Paxil CR CEP holder for the record. Additionally, the data presented in the Paxil CR CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Paxil CR DMF.
A Paxil CR CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Paxil CR 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 Paxil CR suppliers with CEP (COS) on PharmaCompass.
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