01 1Alives Life Sciences Limited
02 1SMS Pharmaceuticals Limited
03 1Syn-Tech Chem. & Pharm. Co. , Ltd.
04 1Tianish Laboratories Private Limited
01 4Rizatriptan benzoate
01 2India
02 1Taiwan
03 1U.S.A
Registration Number : 228MF10064
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Mahara...
Initial Date of Registration : 2016-02-24
Latest Date of Registration : 2019-03-19
Registration Number : 228MF10019
Registrant's Address : Plot No. 72, H. No.:8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills...
Initial Date of Registration : 2016-01-14
Latest Date of Registration : 2016-01-14
Registration Number : 227MF10229
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2015-09-03
Latest Date of Registration : 2015-09-03
Registration Number : 227MF10282
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2015-12-15
Latest Date of Registration : 2016-11-09
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PharmaCompass offers a list of Rizatriptan Benzoate 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 Rizatriptan Benzoate manufacturer or Rizatriptan Benzoate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rizatriptan Benzoate manufacturer or Rizatriptan Benzoate supplier.
PharmaCompass also assists you with knowing the Rizatriptan Benzoate API Price utilized in the formulation of products. Rizatriptan Benzoate API Price is not always fixed or binding as the Rizatriptan Benzoate Price is obtained through a variety of data sources. The Rizatriptan Benzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Maxalt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Maxalt, including repackagers and relabelers. The FDA regulates Maxalt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Maxalt 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 Maxalt manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Maxalt supplier is an individual or a company that provides Maxalt active pharmaceutical ingredient (API) or Maxalt finished formulations upon request. The Maxalt suppliers may include Maxalt API manufacturers, exporters, distributors and traders.
click here to find a list of Maxalt 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 Maxalt Drug Master File in Japan (Maxalt JDMF) empowers Maxalt 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 Maxalt JDMF during the approval evaluation for pharmaceutical products. At the time of Maxalt 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 Maxalt suppliers with JDMF on PharmaCompass.
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