01 1Janssen Pharmaceutica NV
02 1Yung Zip Chemical Ind. Co. , Ltd.
01 2Miconazole nitrate
01 1Taiwan
02 1U.S.A
Registration Number : 219MF10167
Registrant's Address : Turnhoutseweg 30 B-2340 Beerse Belgium
Initial Date of Registration : 2007-05-21
Latest Date of Registration : 2007-05-21
Registration Number : 223MF10006
Registrant's Address : 59, You Shih Road, Youth Industrial District, Dajia, Taichung, Taiwan 43767, R. O. C.
Initial Date of Registration : 2011-01-14
Latest Date of Registration : 2020-05-25
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PharmaCompass offers a list of Miconazole Nitrate 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 Miconazole Nitrate manufacturer or Miconazole Nitrate supplier for your needs.
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PharmaCompass also assists you with knowing the Miconazole Nitrate API Price utilized in the formulation of products. Miconazole Nitrate API Price is not always fixed or binding as the Miconazole Nitrate Price is obtained through a variety of data sources. The Miconazole Nitrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Gyno-Daktarin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Gyno-Daktarin, including repackagers and relabelers. The FDA regulates Gyno-Daktarin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Gyno-Daktarin 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 Gyno-Daktarin supplier is an individual or a company that provides Gyno-Daktarin active pharmaceutical ingredient (API) or Gyno-Daktarin finished formulations upon request. The Gyno-Daktarin suppliers may include Gyno-Daktarin API manufacturers, exporters, distributors and traders.
click here to find a list of Gyno-Daktarin 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 Gyno-Daktarin Drug Master File in Japan (Gyno-Daktarin JDMF) empowers Gyno-Daktarin 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 Gyno-Daktarin JDMF during the approval evaluation for pharmaceutical products. At the time of Gyno-Daktarin 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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