Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
01 1MINAKEM Dunkerque FR
02 2METROCHEM API PRIVATE LIMITED Hyderabad IN
03 1PCAS Ecully FR
04 3DR. REDDY'S LABORATORIES LIMITED Hyderabad IN
05 2LEE PHARMA LIMITED Hyderabad IN
06 1ALIVUS LIFE SCIENCES LIMITED Mumbai IN
07 2APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
08 1CHROMO LABORATORIES INDIA PRIVATE LIMITED Pashamylaram IN
09 2CIPLA LIMITED Mumbai IN
10 1EVEREST ORGANICS LIMITED Aroor Village IN
11 1F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
12 1HEC PHARM CO., LTD. Yidu City CN
13 2HETERO DRUGS LIMITED Hyderabad IN
14 1JIANGSU ZHONGBANG PHARMACEUTICAL CO., LTD. Gaochun CN
15 2JUBILANT PHARMOVA LIMITED Nanjangud IN
16 1KRKA, d.d., Novo mesto Novo mesto SI
17 1LUPIN LIMITED Mumbai IN
18 2MSN LIFE SCIENCES PRIVATE LIMITED Chandampet Village IN
19 1NIFTY LABS PRIVATE LIMITED Hyderabad IN
20 1NINGBO MENOVO PHARMACEUTICAL CO., LTD. Ningbo CN
21 1NINGBO MENOVO PHARMACEUTICAL CO., LTD. Ningbo Hi-Tech District CN
22 5NOSCH LABS PRIVATE LIMITED Hyderabad IN
23 1QILU PHARMACEUTICAL CO., LTD. Jinan CN
24 2QUIMICA SINTETICA S.A. Alcala De Henares ES
25 3SHOUGUANG FUKANG PHARMACEUTICAL CO., LTD. Shouguang City CN
26 1SMILAX LABORATORIES LIMITED Hyderabad IN
27 1SRINI PHARMACEUTICALS PRIVATE LIMITED Choutuppal IN
28 1Sandoz Syntek Ilaç Hammaddeleri Sanayi Ve Ticaret A.S. Istanbul TR
29 2TIANISH LABORATORIES PRIVATE LIMITED Hyderabad IN
30 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
31 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
32 1ZHEJIANG HUAYI PHARMACEUTICAL CO., LTD. Yiwu CN
33 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
Minakem delivers API, HPAPI, steroids & CDMO services for generics with FDA/GMP certification, regulatory know-how & proven success.
Esomeprazole Magnesium Trihydrate, Micronised, N...
Certificate Number : R1-CEP 2012-256 - Rev 02
Status : Valid
Issue Date : 2021-06-03
Type : Chemical
Substance Number : 2372
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Esomeprazole Magnesium Dihydrate
Certificate Number : CEP 2021-022 - Rev 01
Status : Valid
Issue Date : 2024-06-20
Type : Chemical
Substance Number : 2787
Esomeprazole Magnesium Dihydrate, Form A - Micro...
Certificate Number : R1-CEP 2015-043 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2020-12-02
Type : Chemical
Substance Number : 2787
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Esomeprazole Magnesium Trihydrate
Certificate Number : R1-CEP 2012-395 - Rev 01
Status : Valid
Issue Date : 2023-06-05
Type : Chemical
Substance Number : 2372
Lee Pharma Ltd: Global supplier of certified APIs and formulations, driven by innovation and regulatory excellence.
Esomeprazole Magnesium Trihydrate
Certificate Number : CEP 2016-284 - Rev 01
Status : Valid
Issue Date : 2025-07-08
Type : Chemical
Substance Number : 2372
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
Esomeprazole Magnesium Trihydrate
Certificate Number : CEP 2020-386 - Rev 02
Status : Valid
Issue Date : 2024-08-26
Type : Chemical
Substance Number : 2372
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Esomeprazole Magnesium Trihydrate, EMT-2 Process
Certificate Number : R0-CEP 2023-070 - Rev 00
Status : Valid
Issue Date : 2023-06-15
Type : Chemical
Substance Number : 2372
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Esomeprazole Magnesium Trihydrate, Process II
Certificate Number : R0-CEP 2021-243 - Rev 00
Status : Valid
Issue Date : 2022-01-03
Type : Chemical
Substance Number : 2372
Lee Pharma Ltd: Global supplier of certified APIs and formulations, driven by innovation and regulatory excellence.
Esomeprazole Magnesium Dihydrate
Certificate Number : R0-CEP 2021-334 - Rev 00
Status : Valid
Issue Date : 2022-05-03
Type : Chemical
Substance Number : 2787
13
PharmaCompass offers a list of Esomeprazole Magnesium 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 Esomeprazole Magnesium manufacturer or Esomeprazole Magnesium supplier for your needs.
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PharmaCompass also assists you with knowing the Esomeprazole Magnesium API Price utilized in the formulation of products. Esomeprazole Magnesium API Price is not always fixed or binding as the Esomeprazole Magnesium Price is obtained through a variety of data sources. The Esomeprazole Magnesium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VIMOVO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VIMOVO, including repackagers and relabelers. The FDA regulates VIMOVO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VIMOVO 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 VIMOVO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A VIMOVO supplier is an individual or a company that provides VIMOVO active pharmaceutical ingredient (API) or VIMOVO finished formulations upon request. The VIMOVO suppliers may include VIMOVO API manufacturers, exporters, distributors and traders.
click here to find a list of VIMOVO suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A VIMOVO CEP of the European Pharmacopoeia monograph is often referred to as a VIMOVO Certificate of Suitability (COS). The purpose of a VIMOVO CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of VIMOVO EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of VIMOVO to their clients by showing that a VIMOVO CEP has been issued for it. The manufacturer submits a VIMOVO CEP (COS) as part of the market authorization procedure, and it takes on the role of a VIMOVO CEP holder for the record. Additionally, the data presented in the VIMOVO CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the VIMOVO DMF.
A VIMOVO CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. VIMOVO 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 VIMOVO suppliers with CEP (COS) on PharmaCompass.
We have 32 companies offering VIMOVO
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