Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
01 1EGIS Pharmaceuticals PLC Budapest HU
02 1Moehs Iberica S.L. Rubi ES
03 1SCI PHARMTECH, INC. Taoyuan City TW
04 2ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
05 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
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
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
Certificate Number : CEP 2023-144 - Rev 00
Status : Valid
Issue Date : 2024-12-19
Type : Chemical
Substance Number : 2594
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
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PharmaCompass offers a list of Duloxetine 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 Duloxetine manufacturer or Duloxetine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Duloxetine manufacturer or Duloxetine supplier.
PharmaCompass also assists you with knowing the Duloxetine API Price utilized in the formulation of products. Duloxetine API Price is not always fixed or binding as the Duloxetine Price is obtained through a variety of data sources. The Duloxetine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Duloxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duloxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Duloxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duloxetine 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 Duloxetine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duloxetine Hydrochloride supplier is an individual or a company that provides Duloxetine Hydrochloride active pharmaceutical ingredient (API) or Duloxetine Hydrochloride finished formulations upon request. The Duloxetine Hydrochloride suppliers may include Duloxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Duloxetine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Duloxetine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Duloxetine Hydrochloride Certificate of Suitability (COS). The purpose of a Duloxetine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Duloxetine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Duloxetine Hydrochloride to their clients by showing that a Duloxetine Hydrochloride CEP has been issued for it. The manufacturer submits a Duloxetine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Duloxetine Hydrochloride CEP holder for the record. Additionally, the data presented in the Duloxetine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Duloxetine Hydrochloride DMF.
A Duloxetine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Duloxetine 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 Duloxetine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 25 companies offering Duloxetine Hydrochloride
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