01 1Curia Spain S. A. U.
02 1MSD International GmbH (Singapore Branch)
03 1Newchem S. p. A.
04 2Sicor Societa (') Italiana Corticosteroidi S. r. l.
05 1Sicor de Me(´)xico,S. A. de C. V.
01 1Al Black betamethasone propionate "Teva"
02 1Betamethasone Butyrate Propionate
03 1Betamethasone dipropionate
04 1Betamethasone dipropionate "Teva"
05 1Betamethasone dipropionate ester "Teva 2"
06 1Japanese Pharmacopoeia betamethasone dipropionate ester
01 3Italy
02 1Mexico
03 1Singapore
04 1U.S.A
Betamethasone dipropionate (JP)
Registration Number : 219MF10367
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2017-12-08
Registration Number : 218MF10865
Registrant's Address : 50 Tuas West Drive Singapore 638408
Initial Date of Registration : 2006-11-06
Latest Date of Registration : 2014-03-13
Betamethasone Butyrate Propionate
Registration Number : 218MF10277
Registrant's Address : Via de Amicis 47, 20123 Milano, Italy
Initial Date of Registration : 2006-02-28
Latest Date of Registration : 2010-01-07
Alclometasone propionate (Teva)
Registration Number : 218MF10900
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2006-11-10
Latest Date of Registration : 2023-04-19
Betamethasone dipropionate "Teva"
Registration Number : 218MF10459
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2006-04-27
Betamethasone dipropionate "Teva 2"
Registration Number : 225MF10196
Registrant's Address : Piazzale Luigi Cadorna, 4-20123 MILANO, Italy
Initial Date of Registration : 2013-10-23
Latest Date of Registration : 2013-10-23
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PharmaCompass offers a list of Betamethasone Dipropionate 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 Dipropionate manufacturer or Betamethasone Dipropionate supplier for your needs.
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PharmaCompass also assists you with knowing the Betamethasone Dipropionate API Price utilized in the formulation of products. Betamethasone Dipropionate API Price is not always fixed or binding as the Betamethasone Dipropionate Price is obtained through a variety of data sources. The Betamethasone Dipropionate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Rinderon DP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rinderon DP, including repackagers and relabelers. The FDA regulates Rinderon DP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rinderon DP 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 Rinderon DP supplier is an individual or a company that provides Rinderon DP active pharmaceutical ingredient (API) or Rinderon DP finished formulations upon request. The Rinderon DP suppliers may include Rinderon DP API manufacturers, exporters, distributors and traders.
click here to find a list of Rinderon DP 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 Rinderon DP Drug Master File in Japan (Rinderon DP JDMF) empowers Rinderon DP 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 Rinderon DP JDMF during the approval evaluation for pharmaceutical products. At the time of Rinderon DP 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 Rinderon DP suppliers with JDMF on PharmaCompass.
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