Aspen API. More than just an API.
01 1Aspen Oss B. V.
02 1Bayer AG
03 1LABORATORIOS LEON FARMA,S. A.
04 1Zhejiang Xianju Junye Pharmaceutical Co. , Ltd.
01 3Ethinyl estradiol
02 1Ethinyl estradiol betadex
01 1China
02 1Germany
03 1Netherlands
04 1Spain
Aspen API. More than just an API.
Registration Number : 218MF10848
Registrant's Address : Kloosterstraat 6, 5349 AB Oss, the Netherlands
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2007-07-26
Registration Number : 218MF10829
Registrant's Address : Kaiser-Wilhelm-Allee 1,51373 Leverkusen, Germany
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2022-03-30
Registration Number : 303MF10036
Registrant's Address : C/ La Vallina s/n, Poligono Industrial Nabatejera, Villaquilambre, 24008 Leon, Spain
Initial Date of Registration : 2021-02-16
Latest Date of Registration : 2024-01-11
Registration Number : 228MF10156
Registrant's Address : No. 1 Junye Road, Xianju, Taizhou, Zhejiang, China
Initial Date of Registration : 2016-08-10
Latest Date of Registration : 2016-08-10
A Ethinylestradiol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethinylestradiol, including repackagers and relabelers. The FDA regulates Ethinylestradiol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethinylestradiol 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 Ethinylestradiol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ethinylestradiol supplier is an individual or a company that provides Ethinylestradiol active pharmaceutical ingredient (API) or Ethinylestradiol finished formulations upon request. The Ethinylestradiol suppliers may include Ethinylestradiol API manufacturers, exporters, distributors and traders.
click here to find a list of Ethinylestradiol 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 Ethinylestradiol Drug Master File in Japan (Ethinylestradiol JDMF) empowers Ethinylestradiol 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 Ethinylestradiol JDMF during the approval evaluation for pharmaceutical products. At the time of Ethinylestradiol 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 Ethinylestradiol suppliers with JDMF on PharmaCompass.
We have 4 companies offering Ethinylestradiol
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