Axplora is your partner of choice for complex APIs.
01 1Farmabios S. p. A.
02 1Pfizer Inc.
03 1Sogo Pharmaceutical Co., Ltd.
01 2Chlormadinone Acetate
02 1Japanese Pharmacopoeia chlormadinone acetate ester
01 1Germany
02 1Japan
03 1U.S.A
Axplora is your partner of choice for complex APIs.
Registration Number : 218MF10991
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2019-07-04
Japanese Pharmacopoeia Chlormadinone Acetate
Registration Number : 218MF10701
Registrant's Address : 1-8-2 Marunouchi, Chiyoda-ku, Tokyo
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2006-08-11
Registration Number : 217MF10977
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2005-11-14
Latest Date of Registration : 2009-05-27
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PharmaCompass offers a list of Chlormadinone Acetate 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 Chlormadinone Acetate manufacturer or Chlormadinone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlormadinone Acetate manufacturer or Chlormadinone Acetate supplier.
PharmaCompass also assists you with knowing the Chlormadinone Acetate API Price utilized in the formulation of products. Chlormadinone Acetate API Price is not always fixed or binding as the Chlormadinone Acetate Price is obtained through a variety of data sources. The Chlormadinone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lormin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lormin, including repackagers and relabelers. The FDA regulates Lormin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lormin 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 Lormin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lormin supplier is an individual or a company that provides Lormin active pharmaceutical ingredient (API) or Lormin finished formulations upon request. The Lormin suppliers may include Lormin API manufacturers, exporters, distributors and traders.
click here to find a list of Lormin 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 Lormin Drug Master File in Japan (Lormin JDMF) empowers Lormin 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 Lormin JDMF during the approval evaluation for pharmaceutical products. At the time of Lormin 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 Lormin suppliers with JDMF on PharmaCompass.
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