Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1CU Chemie Uetikon GmbH Lahr DE
02 1SUPRIYA LIFESCIENCE LTD. Mumbai IN
03 1AREVIPHARMA GMBH Radebeul DE
04 1MAITHRI DRUGS PRIVATE LIMITED Bonthapally Village IN
01 4Esketamine hydrochloride
01 1France
02 1Germany
03 2India
01 4Valid
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Certificate Number : CEP 2017-216 - Rev 02
Status : Valid
Issue Date : 2023-11-08
Type : Chemical
Substance Number : 1742
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Certificate Number : R0-CEP 2018-198 - Rev 00
Status : Valid
Issue Date : 2021-03-01
Type : Chemical
Substance Number : 1742
Certificate Number : R0-CEP 2022-404 - Rev 00
Status : Valid
Issue Date : 2023-06-21
Type : Chemical
Substance Number : 1742
Certificate Number : CEP 2022-319 - Rev 00
Status : Valid
Issue Date : 2024-05-03
Type : Chemical
Substance Number : 1742
A Esketamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Esketamine, including repackagers and relabelers. The FDA regulates Esketamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Esketamine 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 Esketamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Esketamine supplier is an individual or a company that provides Esketamine active pharmaceutical ingredient (API) or Esketamine finished formulations upon request. The Esketamine suppliers may include Esketamine API manufacturers, exporters, distributors and traders.
click here to find a list of Esketamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Esketamine CEP of the European Pharmacopoeia monograph is often referred to as a Esketamine Certificate of Suitability (COS). The purpose of a Esketamine CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Esketamine EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Esketamine to their clients by showing that a Esketamine CEP has been issued for it. The manufacturer submits a Esketamine CEP (COS) as part of the market authorization procedure, and it takes on the role of a Esketamine CEP holder for the record. Additionally, the data presented in the Esketamine CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Esketamine DMF.
A Esketamine CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Esketamine 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 Esketamine suppliers with CEP (COS) on PharmaCompass.
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