01 1Dishman Carbogen Amcis Ltd.
01 1Handok Co., Ltd.
01 1Eprosartan mesylate
01 1India
Registrant Name : Handok Co., Ltd.
Registration Date : 2021-03-25
Registration Number : 20210325-209-J-911
Manufacturer Name : Dishman Carbogen Amcis Ltd.
Manufacturer Address : Survey No. 47 & 48, Paiki Sub Plot No. 1, Village: Lodariyal, Taluka: Sanand, Dist. A...
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PharmaCompass offers a list of Eprosartan Mesylate 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 Eprosartan Mesylate manufacturer or Eprosartan Mesylate supplier for your needs.
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PharmaCompass also assists you with knowing the Eprosartan Mesylate API Price utilized in the formulation of products. Eprosartan Mesylate API Price is not always fixed or binding as the Eprosartan Mesylate Price is obtained through a variety of data sources. The Eprosartan Mesylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Teveten manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Teveten, including repackagers and relabelers. The FDA regulates Teveten manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Teveten API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Teveten supplier is an individual or a company that provides Teveten active pharmaceutical ingredient (API) or Teveten finished formulations upon request. The Teveten suppliers may include Teveten API manufacturers, exporters, distributors and traders.
click here to find a list of Teveten 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 Teveten Drug Master File in Korea (Teveten KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Teveten. The MFDS reviews the Teveten KDMF as part of the drug registration process and uses the information provided in the Teveten KDMF to evaluate the safety and efficacy of the drug.
After submitting a Teveten 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 Teveten API can apply through the Korea Drug Master File (KDMF).
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