01 1FORMOSA LABORATORIES, INC.
02 1INDUSTRIALE CHIMICA s. r. l.
03 1ScinoPharm Taiwan, Ltd.
01 3Levonorgestrel
01 1Italy
02 2Taiwan
Registration Number : 228MF10159
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2016-08-10
Latest Date of Registration : 2017-02-22
Registration Number : 221MF10183
Registrant's Address : Via E. H. Grieg, 13, 21047 Saronno (Varese) ITALY
Initial Date of Registration : 2009-08-13
Latest Date of Registration : 2023-02-15
Registration Number : 221MF10292
Registrant's Address : No. 1, Nan-Ke 8th Road, Shan-Hua, Tainan 74144 Taiwan
Initial Date of Registration : 2009-12-25
Latest Date of Registration : 2020-07-29
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PharmaCompass offers a list of Levonorgestrel 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 Levonorgestrel manufacturer or Levonorgestrel supplier for your needs.
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PharmaCompass also assists you with knowing the Levonorgestrel API Price utilized in the formulation of products. Levonorgestrel API Price is not always fixed or binding as the Levonorgestrel Price is obtained through a variety of data sources. The Levonorgestrel Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trifeme 28 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trifeme 28, including repackagers and relabelers. The FDA regulates Trifeme 28 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trifeme 28 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Trifeme 28 supplier is an individual or a company that provides Trifeme 28 active pharmaceutical ingredient (API) or Trifeme 28 finished formulations upon request. The Trifeme 28 suppliers may include Trifeme 28 API manufacturers, exporters, distributors and traders.
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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 Trifeme 28 Drug Master File in Japan (Trifeme 28 JDMF) empowers Trifeme 28 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 Trifeme 28 JDMF during the approval evaluation for pharmaceutical products. At the time of Trifeme 28 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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