01 1Dottikon Exclusive Synthesis AG
02 1SMS Pharmaceuticals Limited
01 1Pharmapia Co., Ltd.
02 1SK Chemical Co., Ltd.
01 2Zolmitriptan
01 1India
02 1Switzerland
Registrant Name : SK Chemical Co., Ltd.
Registration Date : 2021-12-08
Registration Number : 20211208-209-J-1173
Manufacturer Name : Dottikon Exclusive Synthesis...
Manufacturer Address : Hembrunnstrasse 17, 5605 Dottikon, Switzerland
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2024-07-17
Registration Number : 20240717-209-J-1634
Manufacturer Name : SMS Pharmaceuticals Limited ...
Manufacturer Address : Unit-II, Plot No. 24 & 24B and 36 & 37, SV Co-Operative Industrial Estate, Bachupally...
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.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Zolmitriptan Drug Master File in Korea (Zolmitriptan KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Zolmitriptan. The MFDS reviews the Zolmitriptan KDMF as part of the drug registration process and uses the information provided in the Zolmitriptan KDMF to evaluate the safety and efficacy of the drug.
After submitting a Zolmitriptan KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Zolmitriptan API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Zolmitriptan suppliers with KDMF on PharmaCompass.
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