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01 2Farmabios S. p. A.
02 1Bayer AG
03 1Tianjin Tianyao Pharmaceuticals Co. , Ltd.
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01 1Diflucortolone Valerate
02 1Diflucortolone Valerate Micronized
03 1Diflucortolone valerate
04 1Valerate diflucortolone
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01 1China
02 3Germany
Diflucortolone Valerate Micronized
Registration Number : 304MF10077
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2022-05-18
Latest Date of Registration : 2022-05-18
Registration Number : 220MF10182
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2008-07-31
Registration Number : 218MF10941
Registrant's Address : Kaiser-Wilhelm-Allee 1,51373 Leverkusen, Germany
Initial Date of Registration : 2006-11-24
Latest Date of Registration : 2006-11-24
Registration Number : 302MF10082
Registrant's Address : No. 19, XINYE 9th Street, West Area of Tianjin Economic-Technological Developme...
Initial Date of Registration : 2020-07-16
Latest Date of Registration : 2020-07-16
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PharmaCompass offers a list of Diflucortolone Valerate 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 Diflucortolone Valerate manufacturer or Diflucortolone Valerate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diflucortolone Valerate manufacturer or Diflucortolone Valerate supplier.
PharmaCompass also assists you with knowing the Diflucortolone Valerate API Price utilized in the formulation of products. Diflucortolone Valerate API Price is not always fixed or binding as the Diflucortolone Valerate Price is obtained through a variety of data sources. The Diflucortolone Valerate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Neriforte manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neriforte, including repackagers and relabelers. The FDA regulates Neriforte manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neriforte 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 Neriforte manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Neriforte supplier is an individual or a company that provides Neriforte active pharmaceutical ingredient (API) or Neriforte finished formulations upon request. The Neriforte suppliers may include Neriforte API manufacturers, exporters, distributors and traders.
click here to find a list of Neriforte 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 Neriforte Drug Master File in Japan (Neriforte JDMF) empowers Neriforte 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 Neriforte JDMF during the approval evaluation for pharmaceutical products. At the time of Neriforte 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 Neriforte suppliers with JDMF on PharmaCompass.
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