01 1Aurobindo Pharma Limited
02 1Glenmark Life Sciences 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 : 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 : 225MF10214
Registrant's Address : Glenmark House, HDO Corporate Building, Wing A, B. D. Sawant Marg, Chakala, Off Weste...
Initial Date of Registration : 2013-11-20
Latest Date of Registration : 2013-11-20
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
A Zolmitriptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolmitriptan, including repackagers and relabelers. The FDA regulates Zolmitriptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolmitriptan 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 Zolmitriptan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolmitriptan supplier is an individual or a company that provides Zolmitriptan active pharmaceutical ingredient (API) or Zolmitriptan finished formulations upon request. The Zolmitriptan suppliers may include Zolmitriptan API manufacturers, exporters, distributors and traders.
click here to find a list of Zolmitriptan 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 Zolmitriptan Drug Master File in Japan (Zolmitriptan JDMF) empowers Zolmitriptan 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 Zolmitriptan JDMF during the approval evaluation for pharmaceutical products. At the time of Zolmitriptan 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 Zolmitriptan suppliers with JDMF on PharmaCompass.
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