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Status : Withdrawn by Holder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
A Liothyronine Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Liothyronine Sodium, including repackagers and relabelers. The FDA regulates Liothyronine Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Liothyronine Sodium 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 Liothyronine Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Liothyronine Sodium supplier is an individual or a company that provides Liothyronine Sodium active pharmaceutical ingredient (API) or Liothyronine Sodium finished formulations upon request. The Liothyronine Sodium suppliers may include Liothyronine Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Liothyronine Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Liothyronine Sodium CEP of the European Pharmacopoeia monograph is often referred to as a Liothyronine Sodium Certificate of Suitability (COS). The purpose of a Liothyronine Sodium CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Liothyronine Sodium EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Liothyronine Sodium to their clients by showing that a Liothyronine Sodium CEP has been issued for it. The manufacturer submits a Liothyronine Sodium CEP (COS) as part of the market authorization procedure, and it takes on the role of a Liothyronine Sodium CEP holder for the record. Additionally, the data presented in the Liothyronine Sodium CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Liothyronine Sodium DMF.
A Liothyronine Sodium CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Liothyronine Sodium 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 Liothyronine Sodium suppliers with CEP (COS) on PharmaCompass.
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