Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Iberica S.L. Rubi ES
02 1NEULAND LABORATORIES LIMITED Hyderabad IN
03 1AREVIPHARMA GMBH Radebeul DE
04 1SIEGFRIED LTD. Zofingen CH
05 1Shaanxi Hanjiang Pharmaceutical Group Co., Ltd. Hanzhong City CN
01 5Sotalol hydrochloride
01 1China
02 1Germany
03 1India
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
Neuland Laboratories- A dedicated 100% API provider.
Neuland Laboratories- A dedicated 100% API provider.
Certificate Number : CEP 2001-269 - Rev 09
Status : Valid
Issue Date : 2024-03-06
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Status : Withdrawn by Holder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Status : Withdrawn by Holder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
A Sotalol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sotalol Hydrochloride, including repackagers and relabelers. The FDA regulates Sotalol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sotalol 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 Sotalol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sotalol Hydrochloride supplier is an individual or a company that provides Sotalol Hydrochloride active pharmaceutical ingredient (API) or Sotalol Hydrochloride finished formulations upon request. The Sotalol Hydrochloride suppliers may include Sotalol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Sotalol Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sotalol Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Sotalol Hydrochloride Certificate of Suitability (COS). The purpose of a Sotalol Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Sotalol Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Sotalol Hydrochloride to their clients by showing that a Sotalol Hydrochloride CEP has been issued for it. The manufacturer submits a Sotalol Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Sotalol Hydrochloride CEP holder for the record. Additionally, the data presented in the Sotalol Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Sotalol Hydrochloride DMF.
A Sotalol Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Sotalol 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 Sotalol Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 5 companies offering Sotalol Hydrochloride
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