01 1SMS Pharmaceuticals Limited
01 1Coapharm Bio Co., Ltd.
01 1Lizatriptan benzoate
01 1India
Registrant Name : Coapharm Bio Co., Ltd.
Registration Date : 2026-01-30
Registration Number : Su152-5-ND
Manufacturer Name : SMS Pharmaceuticals Limited
Manufacturer Address : Unit-Ⅱ, Plot No. 24&24B, 36&37, SVCo-operative Industrial Estate, Bachupally, Medch...
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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, and more, enabling you to easily find the right Rizatriptan Benzoate manufacturer or Rizatriptan Benzoate supplier for your needs.
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A Rizatriptan Benzoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rizatriptan Benzoate, including repackagers and relabelers. The FDA regulates Rizatriptan Benzoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rizatriptan Benzoate 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 Rizatriptan Benzoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Rizatriptan Benzoate supplier is an individual or a company that provides Rizatriptan Benzoate active pharmaceutical ingredient (API) or Rizatriptan Benzoate finished formulations upon request. The Rizatriptan Benzoate suppliers may include Rizatriptan Benzoate API manufacturers, exporters, distributors and traders.
click here to find a list of Rizatriptan Benzoate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Rizatriptan Benzoate Drug Master File in Korea (Rizatriptan Benzoate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Rizatriptan Benzoate. The MFDS reviews the Rizatriptan Benzoate KDMF as part of the drug registration process and uses the information provided in the Rizatriptan Benzoate KDMF to evaluate the safety and efficacy of the drug.
After submitting a Rizatriptan Benzoate 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 Rizatriptan Benzoate API can apply through the Korea Drug Master File (KDMF).
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