Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1AREVIPHARMA GMBH Radebeul DE
03 1NEULAND LABORATORIES LIMITED Hyderabad IN
04 1SIEGFRIED LTD. Zofingen CH
05 1Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. Hanzhong City CN
01 5Sotalol hydrochloride
01 1China
02 1Gabon
03 1Germany
04 1Spain
05 1Switzerland
01 3Valid
02 2Withdrawn by Holder
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Certificate Number : CEP 2002-049 - Rev 08
Status : Valid
Issue Date : 2024-03-12
Type : Chemical
Substance Number : 2004
Certificate Number : CEP 2005-154 - Rev 04
Status : Valid
Issue Date : 2024-02-20
Type : Chemical
Substance Number : 2004
Certificate Number : R1-CEP 2005-295 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2012-09-06
Type : Chemical
Substance Number : 2004
Certificate Number : R1-CEP 2003-196 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2014-09-12
Type : Chemical
Substance Number : 2004
Certificate Number : CEP 2001-269 - Rev 10
Status : Valid
Issue Date : 2025-04-10
Type : Chemical
Substance Number : 2004
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PharmaCompass offers a list of SOTALOL HCI 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 SOTALOL HCI manufacturer or SOTALOL HCI supplier for your needs.
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PharmaCompass also assists you with knowing the SOTALOL HCI API Price utilized in the formulation of products. SOTALOL HCI API Price is not always fixed or binding as the SOTALOL HCI Price is obtained through a variety of data sources. The SOTALOL HCI Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Darob manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Darob, including repackagers and relabelers. The FDA regulates Darob manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Darob 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 Darob manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Darob supplier is an individual or a company that provides Darob active pharmaceutical ingredient (API) or Darob finished formulations upon request. The Darob suppliers may include Darob API manufacturers, exporters, distributors and traders.
click here to find a list of Darob suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Darob CEP of the European Pharmacopoeia monograph is often referred to as a Darob Certificate of Suitability (COS). The purpose of a Darob CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Darob EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Darob to their clients by showing that a Darob CEP has been issued for it. The manufacturer submits a Darob CEP (COS) as part of the market authorization procedure, and it takes on the role of a Darob CEP holder for the record. Additionally, the data presented in the Darob CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Darob DMF.
A Darob CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Darob 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 Darob suppliers with CEP (COS) on PharmaCompass.
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