01 1Amano Enzyme Co., Ltd.
01 1Japanese Pharmacopoeia Aspergillus production galactosidase (production only)
01 1United Kingdom
Japanese Pharmacopoeia β-galactosidase (Aspergillus) (for manufacturing only)
Registration Number : 217MF10683
Registrant's Address : 2-7 Nishiki 1-chome, Naka-ku, Nagoya City, Aichi Prefecture
Initial Date of Registration : 2005-10-07
Latest Date of Registration : 2010-02-12
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PharmaCompass offers a list of Lovastatin 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 Lovastatin manufacturer or Lovastatin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lovastatin manufacturer or Lovastatin supplier.
PharmaCompass also assists you with knowing the Lovastatin API Price utilized in the formulation of products. Lovastatin API Price is not always fixed or binding as the Lovastatin Price is obtained through a variety of data sources. The Lovastatin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lovastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lovastatin, including repackagers and relabelers. The FDA regulates Lovastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lovastatin 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 Lovastatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lovastatin supplier is an individual or a company that provides Lovastatin active pharmaceutical ingredient (API) or Lovastatin finished formulations upon request. The Lovastatin suppliers may include Lovastatin API manufacturers, exporters, distributors and traders.
click here to find a list of Lovastatin 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 Lovastatin Drug Master File in Japan (Lovastatin JDMF) empowers Lovastatin 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 Lovastatin JDMF during the approval evaluation for pharmaceutical products. At the time of Lovastatin 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 Lovastatin suppliers with JDMF on PharmaCompass.
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