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01 1Farmabios S. p. A.
02 1Curia Spain S. A. U.
03 1MSD International GmbH (Singapore Branch)
04 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
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01 1Betamethasone Valerate
02 2Betamethasone valerate
03 1Betamethasone valerate "Teva"
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01 1Germany
02 1Italy
03 1Singapore
04 1U.S.A
Registration Number : 304MF10098
Registrant's Address : Via Pavia, 1-27027 Gropello Cairoli, Pavia, Italy
Initial Date of Registration : 2022-07-06
Latest Date of Registration : 2024-03-21
Registration Number : 222MF10158
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2010-05-24
Latest Date of Registration : 2010-05-24
Registration Number : 218MF10825
Registrant's Address : 50 Tuas West Drive Singapore 638408
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2014-03-13
Registration Number : 218MF10539
Registrant's Address : Piazzale Luigi Cadorna, 4 - 20123 MILANO, Italy
Initial Date of Registration : 2006-06-01
Latest Date of Registration : 2022-09-08
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PharmaCompass offers a list of Betamethasone 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 Betamethasone Valerate manufacturer or Betamethasone Valerate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Betamethasone Valerate manufacturer or Betamethasone Valerate supplier.
PharmaCompass also assists you with knowing the Betamethasone Valerate API Price utilized in the formulation of products. Betamethasone Valerate API Price is not always fixed or binding as the Betamethasone Valerate Price is obtained through a variety of data sources. The Betamethasone Valerate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A BETADERM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BETADERM, including repackagers and relabelers. The FDA regulates BETADERM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BETADERM 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 BETADERM manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A BETADERM supplier is an individual or a company that provides BETADERM active pharmaceutical ingredient (API) or BETADERM finished formulations upon request. The BETADERM suppliers may include BETADERM API manufacturers, exporters, distributors and traders.
click here to find a list of BETADERM 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 BETADERM Drug Master File in Japan (BETADERM JDMF) empowers BETADERM 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 BETADERM JDMF during the approval evaluation for pharmaceutical products. At the time of BETADERM 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 BETADERM suppliers with JDMF on PharmaCompass.
We have 4 companies offering BETADERM
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