01 1Aresko Life Sciences Private Limited
02 1Bayer AG
03 1Zhejiang Xianju Junye Pharmaceutical Co. , Ltd.
01 3Norethisterone
01 1China
02 1Germany
03 1Blank
Registration Number : 219MF10281
Registrant's Address : Kaiser-Wilhelm-Allee 1,51373 Leverkusen, Germany
Initial Date of Registration : 2007-09-10
Latest Date of Registration : 2012-11-28
Registration Number : 228MF10157
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
Registration Number : 306MF10093
Registrant's Address : Village - Sakhanpur, P. O. - Pirumadara - 244715, Tehsil - Ramnagar, Distt. - Nainita...
Initial Date of Registration : 2024-07-03
Latest Date of Registration : 2024-07-03
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PharmaCompass offers a list of Norethisterone 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 Norethisterone manufacturer or Norethisterone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Norethisterone manufacturer or Norethisterone supplier.
PharmaCompass also assists you with knowing the Norethisterone API Price utilized in the formulation of products. Norethisterone API Price is not always fixed or binding as the Norethisterone Price is obtained through a variety of data sources. The Norethisterone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Loestrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loestrin, including repackagers and relabelers. The FDA regulates Loestrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loestrin 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 Loestrin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Loestrin supplier is an individual or a company that provides Loestrin active pharmaceutical ingredient (API) or Loestrin finished formulations upon request. The Loestrin suppliers may include Loestrin API manufacturers, exporters, distributors and traders.
click here to find a list of Loestrin 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 Loestrin Drug Master File in Japan (Loestrin JDMF) empowers Loestrin 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 Loestrin JDMF during the approval evaluation for pharmaceutical products. At the time of Loestrin 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 Loestrin suppliers with JDMF on PharmaCompass.
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