01 1Sichuan Mol Biopharma Co., Ltd.
01 1Iksoo Pharmaceutical Co., Ltd.
01 1Levocloperastine phendisoate
01 1Blank
Registrant Name : Iksoo Pharmaceutical Co., Ltd.
Registration Date : 2022-11-08
Registration Number : 20221108-209-J-1399
Manufacturer Name : Sichuan Mol Biopharma Co., L...
Manufacturer Address : No.51, Industrial Road, Heshan Town, Pujiang, Chengdu
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PharmaCompass offers a list of Levocloperastine Fendizoate 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 Levocloperastine Fendizoate manufacturer or Levocloperastine Fendizoate supplier for your needs.
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PharmaCompass also assists you with knowing the Levocloperastine Fendizoate API Price utilized in the formulation of products. Levocloperastine Fendizoate API Price is not always fixed or binding as the Levocloperastine Fendizoate Price is obtained through a variety of data sources. The Levocloperastine Fendizoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (S)-Cloperastine Fendizoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (S)-Cloperastine Fendizoate, including repackagers and relabelers. The FDA regulates (S)-Cloperastine Fendizoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (S)-Cloperastine Fendizoate 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 (S)-Cloperastine Fendizoate supplier is an individual or a company that provides (S)-Cloperastine Fendizoate active pharmaceutical ingredient (API) or (S)-Cloperastine Fendizoate finished formulations upon request. The (S)-Cloperastine Fendizoate suppliers may include (S)-Cloperastine Fendizoate 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 (S)-Cloperastine Fendizoate Drug Master File in Korea ((S)-Cloperastine Fendizoate KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of (S)-Cloperastine Fendizoate. The MFDS reviews the (S)-Cloperastine Fendizoate KDMF as part of the drug registration process and uses the information provided in the (S)-Cloperastine Fendizoate KDMF to evaluate the safety and efficacy of the drug.
After submitting a (S)-Cloperastine Fendizoate 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 (S)-Cloperastine Fendizoate API can apply through the Korea Drug Master File (KDMF).
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