01 1Newchem S. p. A.
02 1Symbiotica Specialty Ingredients Sdn. Bhd.
03 1Viyash Life Sciences Private Limited
01 2Clobetasone butyric acid ester
02 1Pramipexole hydrochloride hydrate
01 1Italy
02 1Malaysia
03 1U.S.A
Registration Number : 219MF10361
Registrant's Address : Via San Vittore, 39-20123 Milano (Italy)
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2007-12-13
Registration Number : 228MF10101
Registrant's Address : No. 518, Jalan Waja 4, Taman Industry Waja, 09000 Kulim, Kedah Darul Aman, Malaysia
Initial Date of Registration : 2016-05-27
Latest Date of Registration : 2016-05-27
Pramipexole hydrochloride hydrate
Registration Number : 223MF10165
Registrant's Address : Plot No. 290, Srivalli's Corporate, Road No. 6, Kakatiya Hills, Madhapur, Hyderabad-5...
Initial Date of Registration : 2011-11-28
Latest Date of Registration : 2011-11-28
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PharmaCompass offers a list of Clobetasone 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 Clobetasone Butyrate manufacturer or Clobetasone Butyrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clobetasone Butyrate manufacturer or Clobetasone Butyrate supplier.
PharmaCompass also assists you with knowing the Clobetasone Butyrate API Price utilized in the formulation of products. Clobetasone Butyrate API Price is not always fixed or binding as the Clobetasone Butyrate Price is obtained through a variety of data sources. The Clobetasone Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trimovate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimovate, including repackagers and relabelers. The FDA regulates Trimovate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimovate 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 Trimovate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimovate supplier is an individual or a company that provides Trimovate active pharmaceutical ingredient (API) or Trimovate finished formulations upon request. The Trimovate suppliers may include Trimovate API manufacturers, exporters, distributors and traders.
click here to find a list of Trimovate 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 Trimovate Drug Master File in Japan (Trimovate JDMF) empowers Trimovate 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 Trimovate JDMF during the approval evaluation for pharmaceutical products. At the time of Trimovate 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 Trimovate suppliers with JDMF on PharmaCompass.
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