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 Locetar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Locetar, including repackagers and relabelers. The FDA regulates Locetar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Locetar 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 Locetar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Locetar supplier is an individual or a company that provides Locetar active pharmaceutical ingredient (API) or Locetar finished formulations upon request. The Locetar suppliers may include Locetar API manufacturers, exporters, distributors and traders.
click here to find a list of Locetar 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 Locetar Drug Master File in Japan (Locetar JDMF) empowers Locetar 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 Locetar JDMF during the approval evaluation for pharmaceutical products. At the time of Locetar 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 Locetar suppliers with JDMF on PharmaCompass.
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