01 1Guangzhou Hanpu Pharmaceutical Co.,Ltd.
01 1Insung Trading Co., Ltd.
01 1clotrimazole
01 1China
Registrant Name : Insung Trading Co., Ltd.
Registration Date : 2025-02-14
Registration Number : 20250214-211-J-1765
Manufacturer Name : Guangzhou Hanpu Pharmaceutic...
Manufacturer Address : No.9, Jufeng North Road, Aotou Town, Conghua, Guangzhou China
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PharmaCompass offers a list of Clotrimazole 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 Clotrimazole manufacturer or Clotrimazole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clotrimazole manufacturer or Clotrimazole supplier.
PharmaCompass also assists you with knowing the Clotrimazole API Price utilized in the formulation of products. Clotrimazole API Price is not always fixed or binding as the Clotrimazole Price is obtained through a variety of data sources. The Clotrimazole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lotrimin Af manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lotrimin Af, including repackagers and relabelers. The FDA regulates Lotrimin Af manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lotrimin Af 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 Lotrimin Af supplier is an individual or a company that provides Lotrimin Af active pharmaceutical ingredient (API) or Lotrimin Af finished formulations upon request. The Lotrimin Af suppliers may include Lotrimin Af API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Lotrimin Af Drug Master File in Korea (Lotrimin Af KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Lotrimin Af. The MFDS reviews the Lotrimin Af KDMF as part of the drug registration process and uses the information provided in the Lotrimin Af KDMF to evaluate the safety and efficacy of the drug.
After submitting a Lotrimin Af 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 Lotrimin Af API can apply through the Korea Drug Master File (KDMF).
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