IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
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01 1Pharmasynthesis SAS
02 1Zhejiang HISOAR Pharmaceutical Co. ,Ltd
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01 1Amorolfine Hydrochloride
02 1Amorolfine hydrochloride (manufacturing only)
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01 1China
02 1France
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Amorolfine hydrochloride (for manufacturing purposes only)
Registration Number : 303MF10079
Registrant's Address : 57, rue Gravetel St Pierre Les Elbeuf France
Initial Date of Registration : 2021-05-17
Latest Date of Registration : 2021-05-17
Registration Number : 303MF10111
Registrant's Address : No. 100 Waisha Branch Rd. , Jiaojiang, Taizhou, Zhejiang, China
Initial Date of Registration : 2021-07-16
Latest Date of Registration : 2021-07-16
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PharmaCompass offers a list of Amorolfine Hydrochloride 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 Amorolfine Hydrochloride manufacturer or Amorolfine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amorolfine Hydrochloride manufacturer or Amorolfine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Amorolfine Hydrochloride API Price utilized in the formulation of products. Amorolfine Hydrochloride API Price is not always fixed or binding as the Amorolfine Hydrochloride Price is obtained through a variety of data sources. The Amorolfine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Loceryl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loceryl, including repackagers and relabelers. The FDA regulates Loceryl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loceryl 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 Loceryl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Loceryl supplier is an individual or a company that provides Loceryl active pharmaceutical ingredient (API) or Loceryl finished formulations upon request. The Loceryl suppliers may include Loceryl API manufacturers, exporters, distributors and traders.
click here to find a list of Loceryl 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 Loceryl Drug Master File in Japan (Loceryl JDMF) empowers Loceryl 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 Loceryl JDMF during the approval evaluation for pharmaceutical products. At the time of Loceryl 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 Loceryl suppliers with JDMF on PharmaCompass.
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