01 1Active Pharma Inc.
02 1Alives Life Sciences Limited
03 2TAPI Croatia Industries Ltd.
01 3Eszopiclone
02 1Eszopiclone "Teva / PLIVA"
01 2Croatia
02 1India
03 1Japan
Registration Number : 301MF10099
Registrant's Address : 2-36-1 Kanda Jinbocho, Chiyoda-ku, Tokyo
Initial Date of Registration : 2019-11-27
Latest Date of Registration : 2019-11-27
Registration Number : 302MF10028
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2020-02-13
Latest Date of Registration : 2020-02-13
Registration Number : 306MF10171
Registrant's Address : Prudnicka cesta 54, Savski Marof, County Brdovec 10291 Prigorje Brdovecko, Croatia
Initial Date of Registration : 2024-12-25
Latest Date of Registration : 2024-12-25
Registration Number : 228MF10074
Registrant's Address : Prudnicka cesta 54, Savski Marof, County Brdovec 10291 Prigorje Brdovecko, Croatia
Initial Date of Registration : 2016-03-24
Latest Date of Registration : 2022-12-07
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PharmaCompass offers a list of Eszopiclone 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 Eszopiclone manufacturer or Eszopiclone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Eszopiclone manufacturer or Eszopiclone supplier.
PharmaCompass also assists you with knowing the Eszopiclone API Price utilized in the formulation of products. Eszopiclone API Price is not always fixed or binding as the Eszopiclone Price is obtained through a variety of data sources. The Eszopiclone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (S)-Zopiclone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (S)-Zopiclone, including repackagers and relabelers. The FDA regulates (S)-Zopiclone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (S)-Zopiclone 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 (S)-Zopiclone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (S)-Zopiclone supplier is an individual or a company that provides (S)-Zopiclone active pharmaceutical ingredient (API) or (S)-Zopiclone finished formulations upon request. The (S)-Zopiclone suppliers may include (S)-Zopiclone API manufacturers, exporters, distributors and traders.
click here to find a list of (S)-Zopiclone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The (S)-Zopiclone Drug Master File in Japan ((S)-Zopiclone JDMF) empowers (S)-Zopiclone API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the (S)-Zopiclone JDMF during the approval evaluation for pharmaceutical products. At the time of (S)-Zopiclone JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of (S)-Zopiclone suppliers with JDMF on PharmaCompass.
We have 3 companies offering (S)-Zopiclone
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