Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
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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
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01 25Duloxetine hydrochloride
02 1Duloxetine hydrochloride, (IV)
03 1Duloxetine hydrochloride, Milled, micronised
04 1Duloxetine hydrochloride, Process B
05 1Duloxetine hydrochloride, Process II
06 1Duloxetine hydrochloride, Process-K
07 1Duloxetine hydrochloride, Route code JU
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01 6China
02 1Hungary
03 16India
04 1Slovakia
05 1Slovenia
06 4Spain
07 1Taiwan
08 1Blank
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01 2Expired
02 28Valid
03 1Withdrawn by Holder
Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.
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
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.
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
Certificate Number : R1-CEP 2013-016 - Rev 02
Status : Valid
Issue Date : 2021-07-26
Type : Chemical
Substance Number : 2594
Certificate Number : R1-CEP 2015-246 - Rev 00
Status : Valid
Issue Date : 2022-03-01
Type : Chemical
Substance Number : 2594
Certificate Number : CEP 2012-368 - Rev 01
Status : Valid
Issue Date : 2024-07-03
Type : Chemical
Substance Number : 2594
Certificate Number : CEP 2012-247 - Rev 01
Status : Valid
Issue Date : 2024-03-14
Type : Chemical
Substance Number : 2594
Certificate Number : R1-CEP 2014-297 - Rev 00
Status : Valid
Issue Date : 2021-08-05
Type : Chemical
Substance Number : 2594
Duloxetine Hydrochloride, Process B
Certificate Number : R0-CEP 2021-003 - Rev 00
Status : Valid
Issue Date : 2022-10-04
Type : Chemical
Substance Number : 2594
Certificate Number : CEP 2015-155 - Rev 01
Status : Valid
Issue Date : 2024-01-24
Type : Chemical
Substance Number : 2594
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A Cymbalta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cymbalta, including repackagers and relabelers. The FDA regulates Cymbalta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cymbalta 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 Cymbalta supplier is an individual or a company that provides Cymbalta active pharmaceutical ingredient (API) or Cymbalta finished formulations upon request. The Cymbalta suppliers may include Cymbalta API manufacturers, exporters, distributors and traders.
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A Cymbalta CEP of the European Pharmacopoeia monograph is often referred to as a Cymbalta Certificate of Suitability (COS). The purpose of a Cymbalta CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cymbalta EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cymbalta to their clients by showing that a Cymbalta CEP has been issued for it. The manufacturer submits a Cymbalta CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cymbalta CEP holder for the record. Additionally, the data presented in the Cymbalta CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cymbalta DMF.
A Cymbalta CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cymbalta 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 Cymbalta suppliers with CEP (COS) on PharmaCompass.
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