Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1SCI PHARMTECH, INC. Taoyuan City TW
03 2ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
04 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
05 1EGIS Pharmaceuticals PLC Budapest HU
06 1ESTEVE QUIMICA S.A. Barcelona ES
07 1HETERO DRUGS LIMITED Hyderabad IN
08 1JUBILANT PHARMOVA LIMITED Nanjangud IN
09 1KRKA, d.d., Novo mesto Novo mesto SI
10 1LUPIN LIMITED Mumbai IN
11 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
12 2MSN LABORATORIES PRIVATE LIMITED Rudraram Village IN
13 2NOSCH LABS PRIVATE LIMITED Hyderabad IN
14 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
15 1R L FINE CHEM PVT. LTD. Gowribidanur IN
16 1SANECA PHARMACEUTICALS A.S. Hlohovec SK
17 1SHODHANA LABORATORIES LIMITED Hyderabad IN
18 1TAPI NL B.V. Amsterdam NL
19 1TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
20 2Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
21 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD. Linhai CN
22 1ZHEJIANG HUAYI PHARMACEUTICAL CO., LTD. Yiwu CN
23 1ZHEJIANG YONGTAI PHARMACEUTICAL CO., LTD. Duqiao CN
24 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
25 1Zhejiang Jiuzhou Pharmaceutical Co., Ltd. Taizhou City CN
26 1Zhejiang Liaoyuan Pharmaceutical Co., Ltd. Duqiao Town CN
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Duloxetine Hydrochloride, Milled, Micronised
Certificate Number : CEP 2012-319 - Rev 01
Status : Valid
Issue Date : 2024-06-21
Type : Chemical
Substance Number : 2594
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Certificate Number : R1-CEP 2012-217 - Rev 01
Status : Valid
Issue Date : 2022-09-21
Type : Chemical
Substance Number : 2594
A Duloxetine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duloxetine, including repackagers and relabelers. The FDA regulates Duloxetine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duloxetine 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 Duloxetine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duloxetine supplier is an individual or a company that provides Duloxetine active pharmaceutical ingredient (API) or Duloxetine finished formulations upon request. The Duloxetine suppliers may include Duloxetine API manufacturers, exporters, distributors and traders.
click here to find a list of Duloxetine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Duloxetine CEP of the European Pharmacopoeia monograph is often referred to as a Duloxetine Certificate of Suitability (COS). The purpose of a Duloxetine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Duloxetine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Duloxetine to their clients by showing that a Duloxetine CEP has been issued for it. The manufacturer submits a Duloxetine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Duloxetine CEP holder for the record. Additionally, the data presented in the Duloxetine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Duloxetine DMF.
A Duloxetine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Duloxetine 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 Duloxetine suppliers with CEP (COS) on PharmaCompass.
We have 24 companies offering Duloxetine
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