IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
01 1Pharmasynthesis SAS
02 1Zhejiang HISOAR Pharmaceutical Co. ,Ltd
01 1Amorolfine Hydrochloride
02 1Amorolfine hydrochloride (manufacturing only)
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
A Amorolfine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amorolfine, including repackagers and relabelers. The FDA regulates Amorolfine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amorolfine 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 Amorolfine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amorolfine supplier is an individual or a company that provides Amorolfine active pharmaceutical ingredient (API) or Amorolfine finished formulations upon request. The Amorolfine suppliers may include Amorolfine API manufacturers, exporters, distributors and traders.
click here to find a list of Amorolfine 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 Amorolfine Drug Master File in Japan (Amorolfine JDMF) empowers Amorolfine 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 Amorolfine JDMF during the approval evaluation for pharmaceutical products. At the time of Amorolfine 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 Amorolfine suppliers with JDMF on PharmaCompass.
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