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01 1Fermion Oy
02 1CHONGQING KANGLE PHARMACEUTICAL CO. , LTD.
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01 2Hydroxychloroquine Sulfate
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01 1China
02 1Finland
Registration Number : 305MF10090
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2023-08-02
Latest Date of Registration : 2023-08-02
Registration Number : 305MF10077
Registrant's Address : No. 4 HUAZHONG ROAD, CHONGQING (CHANGSHOU) CHEMICAL INDUSTRIAL PARK
Initial Date of Registration : 2023-07-05
Latest Date of Registration : 2023-07-05
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PharmaCompass offers a list of Hydroxychloroquine Sulphate 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 Hydroxychloroquine Sulphate manufacturer or Hydroxychloroquine Sulphate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydroxychloroquine Sulphate manufacturer or Hydroxychloroquine Sulphate supplier.
PharmaCompass also assists you with knowing the Hydroxychloroquine Sulphate API Price utilized in the formulation of products. Hydroxychloroquine Sulphate API Price is not always fixed or binding as the Hydroxychloroquine Sulphate Price is obtained through a variety of data sources. The Hydroxychloroquine Sulphate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxychloroquine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxychloroquine, including repackagers and relabelers. The FDA regulates Oxychloroquine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxychloroquine 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 Oxychloroquine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxychloroquine supplier is an individual or a company that provides Oxychloroquine active pharmaceutical ingredient (API) or Oxychloroquine finished formulations upon request. The Oxychloroquine suppliers may include Oxychloroquine API manufacturers, exporters, distributors and traders.
click here to find a list of Oxychloroquine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Oxychloroquine Drug Master File in Japan (Oxychloroquine JDMF) empowers Oxychloroquine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Oxychloroquine JDMF during the approval evaluation for pharmaceutical products. At the time of Oxychloroquine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Oxychloroquine suppliers with JDMF on PharmaCompass.
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