01 1Curia Spain S. A. U.
02 1Newchem S. p. A.
03 1STEROID S. p. A.
01 2Hydrocortisone butyrate
02 1Japanese Pharmacopoeia hydrocortisone butyrate (production only)
01 2Italy
02 1U.S.A
Registration Number : 222MF10284
Registrant's Address : Parque Tecnologico-Parcela 105 Boecillo (Valladolid) Spain
Initial Date of Registration : 2010-12-27
Latest Date of Registration : 2020-04-02
Registration Number : 223MF10022
Registrant's Address : Via de Amicis 47, 20123 Milano, Italy
Initial Date of Registration : 2011-02-08
Latest Date of Registration : 2011-02-08
Japanese Pharmacopoeia Hydrocortisone Butyrate (For manufacturing only)
Registration Number : 222MF10261
Registrant's Address : Viale Spagna, 156 Cologno Monzese (MI) - ITALY
Initial Date of Registration : 2010-11-29
Latest Date of Registration : 2010-11-29
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PharmaCompass offers a list of Hydrocortisone Butyrate 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 Hydrocortisone Butyrate manufacturer or Hydrocortisone Butyrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Hydrocortisone Butyrate manufacturer or Hydrocortisone Butyrate supplier.
PharmaCompass also assists you with knowing the Hydrocortisone Butyrate API Price utilized in the formulation of products. Hydrocortisone Butyrate API Price is not always fixed or binding as the Hydrocortisone Butyrate Price is obtained through a variety of data sources. The Hydrocortisone Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Hydrocortisone Probutate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Probutate, including repackagers and relabelers. The FDA regulates Hydrocortisone Probutate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Probutate 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 Hydrocortisone Probutate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Probutate supplier is an individual or a company that provides Hydrocortisone Probutate active pharmaceutical ingredient (API) or Hydrocortisone Probutate finished formulations upon request. The Hydrocortisone Probutate suppliers may include Hydrocortisone Probutate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Probutate 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 Hydrocortisone Probutate Drug Master File in Japan ( Hydrocortisone Probutate JDMF) empowers Hydrocortisone Probutate 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 Hydrocortisone Probutate JDMF during the approval evaluation for pharmaceutical products. At the time of Hydrocortisone Probutate 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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