01 1Alives Life Sciences Limited
02 1Aurobindo Pharma Limited
03 1JUBILANT PHARMOVA LIMITED
04 1Permakem Asia Co., Ltd.
05 1Syn-Tech Chem. & Pharm. Co. , Ltd.
01 5Zolmitriptan
01 3India
02 1Japan
03 1Taiwan
Registration Number : 225MF10214
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2013-11-20
Latest Date of Registration : 2013-11-20
Registration Number : 226MF10010
Registrant's Address : Plot No. 2, Maitrivihar, Ameerpet, Hyderabad Andhra Pradesh, India
Initial Date of Registration : 2014-01-08
Latest Date of Registration : 2014-11-17
Registration Number : 226MF10053
Registrant's Address : 1A, Sector 16A, Noida 201 301, Uttar Pradesh, India
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2014-11-17
Registration Number : 227MF10076
Registrant's Address : 1-10-11 Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2015-03-12
Latest Date of Registration : 2015-03-12
Registration Number : 226MF10060
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2014-03-06
Latest Date of Registration : 2018-04-17
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PharmaCompass offers a list of Zolmitriptan 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 Zolmitriptan manufacturer or Zolmitriptan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zolmitriptan manufacturer or Zolmitriptan supplier.
PharmaCompass also assists you with knowing the Zolmitriptan API Price utilized in the formulation of products. Zolmitriptan API Price is not always fixed or binding as the Zolmitriptan Price is obtained through a variety of data sources. The Zolmitriptan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Nomi manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nomi, including repackagers and relabelers. The FDA regulates Nomi manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nomi 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 Nomi manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nomi supplier is an individual or a company that provides Nomi active pharmaceutical ingredient (API) or Nomi finished formulations upon request. The Nomi suppliers may include Nomi API manufacturers, exporters, distributors and traders.
click here to find a list of Nomi 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 Nomi Drug Master File in Japan (Nomi JDMF) empowers Nomi 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 Nomi JDMF during the approval evaluation for pharmaceutical products. At the time of Nomi 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 Nomi suppliers with JDMF on PharmaCompass.
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