Aspen API. More than just an API™
01 1Aspen Oss B. V.
02 1Valdepharm
01 1Norethisterone acetate
02 1norethisterone acetate
01 1Luxembourg
02 1Netherlands
Aspen API. More than just an API™
Registration Number : 218MF10585
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2006-06-22
Latest Date of Registration : 2019-10-01
Registration Number : 230MF10159
Registrant's Address : Parc Industriel d'Incarville Parc de la Fringale CS 10606 27106 Val de Reuil Cedex Fr...
Initial Date of Registration : 2018-11-28
Latest Date of Registration : 2021-02-10
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PharmaCompass offers a list of Norethisterone 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 Norethisterone Acetate manufacturer or Norethisterone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Norethisterone Acetate manufacturer or Norethisterone Acetate supplier.
PharmaCompass also assists you with knowing the Norethisterone Acetate API Price utilized in the formulation of products. Norethisterone Acetate API Price is not always fixed or binding as the Norethisterone Acetate Price is obtained through a variety of data sources. The Norethisterone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LO-BLISOVI FE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LO-BLISOVI FE, including repackagers and relabelers. The FDA regulates LO-BLISOVI FE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LO-BLISOVI FE 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 LO-BLISOVI FE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LO-BLISOVI FE supplier is an individual or a company that provides LO-BLISOVI FE active pharmaceutical ingredient (API) or LO-BLISOVI FE finished formulations upon request. The LO-BLISOVI FE suppliers may include LO-BLISOVI FE API manufacturers, exporters, distributors and traders.
click here to find a list of LO-BLISOVI FE 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 LO-BLISOVI FE Drug Master File in Japan (LO-BLISOVI FE JDMF) empowers LO-BLISOVI FE 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 LO-BLISOVI FE JDMF during the approval evaluation for pharmaceutical products. At the time of LO-BLISOVI FE 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 LO-BLISOVI FE suppliers with JDMF on PharmaCompass.
