01 1Heyl Chemisch-pharmazeutische Fabrik GmbH & Co. K.G.
02 1INDUSTRIALE CHIMICA s. r. l.
03 1Newchem S. p. A.
04 1Sterling S. p. A.
01 4Dienogest
01 1Austria
02 3Italy
Registration Number : 227MF10213
Registrant's Address : Via E. H. Grieg, 13,21047 Saronno (VARESE) ITALY
Initial Date of Registration : 2015-08-31
Latest Date of Registration : 2020-09-17
Registration Number : 306MF10159
Registrant's Address : Via San Vittore, 39 - 20123 Milano (Italy)
Initial Date of Registration : 2024-12-18
Latest Date of Registration : 2024-12-18
Registration Number : 228MF10027
Registrant's Address : Kurfu(¨)rstendamm 178-179 10707 Berlin, Germany
Initial Date of Registration : 2016-02-02
Latest Date of Registration : 2016-02-02
Registration Number : 228MF10063
Registrant's Address : Via Della Carboneria 30 Solomeo 06073 Corciano Perugia-Italy
Initial Date of Registration : 2016-02-24
Latest Date of Registration : 2016-02-24
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PharmaCompass offers a list of Dienogest 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 Dienogest manufacturer or Dienogest supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dienogest manufacturer or Dienogest supplier.
PharmaCompass also assists you with knowing the Dienogest API Price utilized in the formulation of products. Dienogest API Price is not always fixed or binding as the Dienogest Price is obtained through a variety of data sources. The Dienogest Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dienogestum manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dienogestum, including repackagers and relabelers. The FDA regulates Dienogestum manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dienogestum 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 Dienogestum manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dienogestum supplier is an individual or a company that provides Dienogestum active pharmaceutical ingredient (API) or Dienogestum finished formulations upon request. The Dienogestum suppliers may include Dienogestum API manufacturers, exporters, distributors and traders.
click here to find a list of Dienogestum 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 Dienogestum Drug Master File in Japan (Dienogestum JDMF) empowers Dienogestum 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 Dienogestum JDMF during the approval evaluation for pharmaceutical products. At the time of Dienogestum 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 Dienogestum suppliers with JDMF on PharmaCompass.
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