01 1AZICO BIOPHORE INDIA PRIVATE LIMITED Anakapalli IN
02 1Peptido GmbH Bexbach DE
03 1SANDOZ GMBH Kundl AT
01 3Liothyronine sodium
01 2Germany
02 1India
01 2Valid
02 1Withdrawn by Holder
Certificate Number : CEP 2017-035 - Rev 01
Status : Valid
Issue Date : 2023-11-29
Type : Chemical and TSE
Substance Number : 728
Certificate Number : R1-CEP 2006-249 - Rev 02
Status : Valid
Issue Date : 2023-07-05
Type : Chemical
Substance Number : 728
Certificate Number : R1-CEP 2001-043 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2008-07-22
Type : Chemical
Substance Number : 728
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PharmaCompass offers a list of Liothyronine Sodium 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 Liothyronine Sodium manufacturer or Liothyronine Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Liothyronine Sodium API Price utilized in the formulation of products. Liothyronine Sodium API Price is not always fixed or binding as the Liothyronine Sodium Price is obtained through a variety of data sources. The Liothyronine Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cynomel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cynomel, including repackagers and relabelers. The FDA regulates Cynomel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cynomel 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 Cynomel supplier is an individual or a company that provides Cynomel active pharmaceutical ingredient (API) or Cynomel finished formulations upon request. The Cynomel suppliers may include Cynomel API manufacturers, exporters, distributors and traders.
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A Cynomel CEP of the European Pharmacopoeia monograph is often referred to as a Cynomel Certificate of Suitability (COS). The purpose of a Cynomel CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Cynomel EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Cynomel to their clients by showing that a Cynomel CEP has been issued for it. The manufacturer submits a Cynomel CEP (COS) as part of the market authorization procedure, and it takes on the role of a Cynomel CEP holder for the record. Additionally, the data presented in the Cynomel CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Cynomel DMF.
A Cynomel CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Cynomel 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 Cynomel suppliers with CEP (COS) on PharmaCompass.
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