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 Lotrimin AF Powder manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lotrimin AF Powder, including repackagers and relabelers. The FDA regulates Lotrimin AF Powder manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lotrimin AF Powder 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 Lotrimin AF Powder supplier is an individual or a company that provides Lotrimin AF Powder active pharmaceutical ingredient (API) or Lotrimin AF Powder finished formulations upon request. The Lotrimin AF Powder suppliers may include Lotrimin AF Powder 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 Lotrimin AF Powder Drug Master File in Japan (Lotrimin AF Powder JDMF) empowers Lotrimin AF Powder 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 Lotrimin AF Powder JDMF during the approval evaluation for pharmaceutical products. At the time of Lotrimin AF Powder 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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