Aspen API. More than just an API.
01 1Aspen Oss B. V.
02 3INDUSTRIALE CHIMICA s. r. l.
01 4Desogestrel
01 3Italy
02 1Netherlands
Aspen API. More than just an API.
Registration Number : 303MF10070
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2021-04-22
Latest Date of Registration : 2021-04-22
Registration Number : 221MF10126
Registrant's Address : Via E. H. Greig, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2009-06-23
Latest Date of Registration : 2009-06-23
Registration Number : 221MF10125
Registrant's Address : Via E. H. Greig, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2009-06-23
Latest Date of Registration : 2009-06-23
Registration Number : 230MF10041
Registrant's Address : Via E. H. Grieg, 13, 21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2018-02-28
Latest Date of Registration : 2018-02-28
A Desogestrel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desogestrel, including repackagers and relabelers. The FDA regulates Desogestrel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desogestrel 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 Desogestrel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desogestrel supplier is an individual or a company that provides Desogestrel active pharmaceutical ingredient (API) or Desogestrel finished formulations upon request. The Desogestrel suppliers may include Desogestrel API manufacturers, exporters, distributors and traders.
click here to find a list of Desogestrel 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 Desogestrel Drug Master File in Japan (Desogestrel JDMF) empowers Desogestrel 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 Desogestrel JDMF during the approval evaluation for pharmaceutical products. At the time of Desogestrel 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 Desogestrel suppliers with JDMF on PharmaCompass.
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