Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
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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
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01 4Esketamine hydrochloride
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01 1France
02 1Germany
03 2India
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01 4Valid
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
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
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PharmaCompass offers a list of Esketamine Hydrochloride 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 Esketamine Hydrochloride manufacturer or Esketamine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Esketamine Hydrochloride manufacturer or Esketamine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Esketamine Hydrochloride API Price utilized in the formulation of products. Esketamine Hydrochloride API Price is not always fixed or binding as the Esketamine Hydrochloride Price is obtained through a variety of data sources. The Esketamine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Esketamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Esketamine Hydrochloride, including repackagers and relabelers. The FDA regulates Esketamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Esketamine 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 Esketamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Esketamine Hydrochloride supplier is an individual or a company that provides Esketamine Hydrochloride active pharmaceutical ingredient (API) or Esketamine Hydrochloride finished formulations upon request. The Esketamine Hydrochloride suppliers may include Esketamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Esketamine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Esketamine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Esketamine Hydrochloride Certificate of Suitability (COS). The purpose of a Esketamine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Esketamine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Esketamine Hydrochloride to their clients by showing that a Esketamine Hydrochloride CEP has been issued for it. The manufacturer submits a Esketamine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Esketamine Hydrochloride CEP holder for the record. Additionally, the data presented in the Esketamine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Esketamine Hydrochloride DMF.
A Esketamine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Esketamine 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 Esketamine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Esketamine Hydrochloride
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