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 Visanne manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Visanne, including repackagers and relabelers. The FDA regulates Visanne manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Visanne 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 Visanne manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Visanne supplier is an individual or a company that provides Visanne active pharmaceutical ingredient (API) or Visanne finished formulations upon request. The Visanne suppliers may include Visanne API manufacturers, exporters, distributors and traders.
click here to find a list of Visanne 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 Visanne Drug Master File in Japan (Visanne JDMF) empowers Visanne 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 Visanne JDMF during the approval evaluation for pharmaceutical products. At the time of Visanne 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 Visanne suppliers with JDMF on PharmaCompass.
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