Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1AMOLI ORGANICS PRIVATE LIMITED Mumbai IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1AUROBINDO PHARMA LIMITED Hyderabad IN
05 1CIPLA LIMITED Mumbai IN
06 2DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
07 4HETERO DRUGS LIMITED Hyderabad IN
08 1LEE PHARMA LIMITED Hyderabad IN
09 1LUPIN LIMITED Mumbai IN
10 1NATCO PHARMA LIMITED Hyderabad IN
11 1NOSCH LABS PRIVATE LIMITED Hyderabad IN
12 2SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
13 1SYMED LABS LIMITED Hyderabad IN
14 1Sandoz Syntek Ilaç Hammaddeleri Sanayi Ve Ticaret A.S. Istanbul TR
15 3TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
16 2TYCHE INDUSTRIES LIMITED Hyderabad IN
17 1VERDANT LIFE SCIENCES PVT., LIMITED Visakhapatnam IN
18 2Wanbury Limited Vashi, Navi Mumbai IN
01 12Sertraline hydrochloride
02 1Sertraline hydrochloride, Alternate process
03 2Sertraline hydrochloride, Form I
04 3Sertraline hydrochloride, Form II
05 4Sertraline hydrochloride, Form-I
06 1Sertraline hydrochloride, Form-II
07 1Sertraline hydrochloride, Form-II, Process-II
08 1Sertraline hydrochloride, Process II
09 1Sertraline hydrochloride, Process IVB
10 1Sertraline hydrochloride, Process-II
01 1Germany
02 25India
03 1Spain
01 1Expired
02 21Valid
03 5Withdrawn by Holder
Certificate Number : R1-CEP 2013-124 - Rev 00
Status : Valid
Issue Date : 2019-06-24
Type : Chemical
Substance Number : 1705
Sertraline Hydrochloride, Form-I
Certificate Number : CEP 2021-424 - Rev 01
Status : Valid
Issue Date : 2024-11-15
Type : Chemical
Substance Number : 1705
Sertraline Hydrochloride, Form-I
Certificate Number : R1-CEP 2012-292 - Rev 02
Status : Valid
Issue Date : 2023-08-25
Type : Chemical
Substance Number : 1705
Certificate Number : R1-CEP 2009-115 - Rev 02
Status : Valid
Issue Date : 2016-09-13
Type : Chemical
Substance Number : 1705
Certificate Number : R1-CEP 2008-265 - Rev 01
Status : Valid
Issue Date : 2020-05-27
Type : Chemical
Substance Number : 1705
Certificate Number : CEP 2008-304 - Rev 04
Status : Valid
Issue Date : 2024-07-18
Type : Chemical
Substance Number : 1705
Certificate Number : CEP 2018-292 - Rev 03
Status : Valid
Issue Date : 2024-11-19
Type : Chemical
Substance Number : 1705
Sertraline Hydrochloride, Form II
Certificate Number : R0-CEP 2022-313 - Rev 00
Status : Valid
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 1705
Certificate Number : R0-CEP 2022-191 - Rev 00
Status : Valid
Issue Date : 2023-08-31
Type : Chemical
Substance Number : 1705
Certificate Number : R1-CEP 2008-173 - Rev 06
Status : Valid
Issue Date : 2022-04-08
Type : Chemical
Substance Number : 1705
A Sertraline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sertraline Hydrochloride, including repackagers and relabelers. The FDA regulates Sertraline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sertraline 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 Sertraline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sertraline Hydrochloride supplier is an individual or a company that provides Sertraline Hydrochloride active pharmaceutical ingredient (API) or Sertraline Hydrochloride finished formulations upon request. The Sertraline Hydrochloride suppliers may include Sertraline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Sertraline Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sertraline Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Sertraline Hydrochloride Certificate of Suitability (COS). The purpose of a Sertraline Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sertraline Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sertraline Hydrochloride to their clients by showing that a Sertraline Hydrochloride CEP has been issued for it. The manufacturer submits a Sertraline Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sertraline Hydrochloride CEP holder for the record. Additionally, the data presented in the Sertraline Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sertraline Hydrochloride DMF.
A Sertraline Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sertraline 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 Sertraline Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 16 companies offering Sertraline Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?