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, 24193 Leon, Spain
Initial Date of Registration : 2021-02-16
Latest Date of Registration : 2024-12-18
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
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PharmaCompass offers a list of Ethinyl Estradiol 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 Ethinyl Estradiol manufacturer or Ethinyl Estradiol supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ethinyl Estradiol manufacturer or Ethinyl Estradiol supplier.
PharmaCompass also assists you with knowing the Ethinyl Estradiol API Price utilized in the formulation of products. Ethinyl Estradiol API Price is not always fixed or binding as the Ethinyl Estradiol Price is obtained through a variety of data sources. The Ethinyl Estradiol Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FALMINA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FALMINA, including repackagers and relabelers. The FDA regulates FALMINA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FALMINA 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 FALMINA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A FALMINA supplier is an individual or a company that provides FALMINA active pharmaceutical ingredient (API) or FALMINA finished formulations upon request. The FALMINA suppliers may include FALMINA API manufacturers, exporters, distributors and traders.
click here to find a list of FALMINA 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 FALMINA Drug Master File in Japan (FALMINA JDMF) empowers FALMINA 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 FALMINA JDMF during the approval evaluation for pharmaceutical products. At the time of FALMINA 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 FALMINA suppliers with JDMF on PharmaCompass.
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