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 PRIVATE LIMITED Anakapalli IN
18 2Wanbury Limited Vashi, Navi Mumbai IN
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : R1-CEP 2013-124 - Rev 00
Status : Valid
Issue Date : 2019-06-24
Type : Chemical
Substance Number : 1705
95
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A SERTRALINE HCL FORM II manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SERTRALINE HCL FORM II, including repackagers and relabelers. The FDA regulates SERTRALINE HCL FORM II manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SERTRALINE HCL FORM II 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 SERTRALINE HCL FORM II supplier is an individual or a company that provides SERTRALINE HCL FORM II active pharmaceutical ingredient (API) or SERTRALINE HCL FORM II finished formulations upon request. The SERTRALINE HCL FORM II suppliers may include SERTRALINE HCL FORM II API manufacturers, exporters, distributors and traders.
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A SERTRALINE HCL FORM II CEP of the European Pharmacopoeia monograph is often referred to as a SERTRALINE HCL FORM II Certificate of Suitability (COS). The purpose of a SERTRALINE HCL FORM II CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of SERTRALINE HCL FORM II EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of SERTRALINE HCL FORM II to their clients by showing that a SERTRALINE HCL FORM II CEP has been issued for it. The manufacturer submits a SERTRALINE HCL FORM II CEP (COS) as part of the market authorization procedure, and it takes on the role of a SERTRALINE HCL FORM II CEP holder for the record. Additionally, the data presented in the SERTRALINE HCL FORM II CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the SERTRALINE HCL FORM II DMF.
A SERTRALINE HCL FORM II CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. SERTRALINE HCL FORM II CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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We have 15 companies offering SERTRALINE HCL FORM II
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