01 1CENTAUR PHARMACEUTICALS PRIVATE LTD.
02 1Cambrex Profarmaco Milano S. r. l.
03 1Ohara Pharmaceutical Co., Ltd.
01 3Brotizolam
01 1India
02 1Japan
03 1U.S.A
Registration Number : 219MF10021
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2007-01-22
Latest Date of Registration : 2021-07-02
Registration Number : 225MF10082
Registrant's Address : “CENTAUR HOUSE”, NEAR GRAND HYATT, SHANTI NAGAR, VAKOLA, SANTACRUZ (EAST), MUMBAI...
Initial Date of Registration : 2013-04-23
Latest Date of Registration : 2013-04-23
Registration Number : 217MF11218
Registrant's Address : 121-15 Toriiino, Koka-cho, Koka City, Shiga Prefecture
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-03-09
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PharmaCompass offers a list of Brotizolam 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 Brotizolam manufacturer or Brotizolam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Brotizolam manufacturer or Brotizolam supplier.
PharmaCompass also assists you with knowing the Brotizolam API Price utilized in the formulation of products. Brotizolam API Price is not always fixed or binding as the Brotizolam Price is obtained through a variety of data sources. The Brotizolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mederantil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mederantil, including repackagers and relabelers. The FDA regulates Mederantil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mederantil 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 Mederantil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Mederantil supplier is an individual or a company that provides Mederantil active pharmaceutical ingredient (API) or Mederantil finished formulations upon request. The Mederantil suppliers may include Mederantil API manufacturers, exporters, distributors and traders.
click here to find a list of Mederantil 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 Mederantil Drug Master File in Japan (Mederantil JDMF) empowers Mederantil 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 Mederantil JDMF during the approval evaluation for pharmaceutical products. At the time of Mederantil 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 Mederantil suppliers with JDMF on PharmaCompass.
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