Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
01 1Pharmaceutical Works POLPHARMA S. A.
02 2Permakem Asia Co., Ltd.
03 1Ryoto Fine Co., Ltd.
04 1Tianish Laboratories Private Limited
01 1Sildenafil Citrate
02 4Sildenafil citrate
01 3Japan
02 1Poland
03 1U.S.A
Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.
Registration Number : 225MF10011
Registrant's Address : 19 Pellinska Str. 83-200 Starogard Gdanski POLAND
Initial Date of Registration : 2013-01-30
Latest Date of Registration : 2020-12-23
Registration Number : 225MF10131
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2013-07-16
Latest Date of Registration : 2013-07-16
Registration Number : 225MF10095
Registrant's Address : 1-10-11, Nihonbashi Horidomecho, Chuo-ku, Tokyo
Initial Date of Registration : 2013-05-08
Latest Date of Registration : 2013-05-08
Registration Number : 225MF10016
Registrant's Address : 1410 Takada, Kashiwa City, Chiba Prefecture
Initial Date of Registration : 2013-02-05
Latest Date of Registration : 2014-10-27
Registration Number : 224MF10197
Registrant's Address : Plot No. 564/A/22, Road No. 92, Jubilee Hills, Hyderabad-500096, Telangana, India
Initial Date of Registration : 2012-09-11
Latest Date of Registration : 2019-07-05
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PharmaCompass offers a list of Sildenafil Citrate 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 Sildenafil Citrate manufacturer or Sildenafil Citrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sildenafil Citrate manufacturer or Sildenafil Citrate supplier.
PharmaCompass also assists you with knowing the Sildenafil Citrate API Price utilized in the formulation of products. Sildenafil Citrate API Price is not always fixed or binding as the Sildenafil Citrate Price is obtained through a variety of data sources. The Sildenafil Citrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sildenafil Citrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sildenafil Citrate, including repackagers and relabelers. The FDA regulates Sildenafil Citrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sildenafil Citrate 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 Sildenafil Citrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sildenafil Citrate supplier is an individual or a company that provides Sildenafil Citrate active pharmaceutical ingredient (API) or Sildenafil Citrate finished formulations upon request. The Sildenafil Citrate suppliers may include Sildenafil Citrate API manufacturers, exporters, distributors and traders.
click here to find a list of Sildenafil Citrate 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 Sildenafil Citrate Drug Master File in Japan (Sildenafil Citrate JDMF) empowers Sildenafil Citrate 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 Sildenafil Citrate JDMF during the approval evaluation for pharmaceutical products. At the time of Sildenafil Citrate 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 Sildenafil Citrate suppliers with JDMF on PharmaCompass.
We have 4 companies offering Sildenafil Citrate
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