01 1HETERO DRUGS LIMITED.
01 1Lurasidone Hydrochloride
01 1India
Registration Number : 304MF10151
Registrant's Address : 7-2-A2, Hetero Corporate, Industrial Estates, Sanath Nagar, Hyderabad-500 018, Telang...
Initial Date of Registration : 2022-12-07
Latest Date of Registration : 2022-12-07
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PharmaCompass offers a list of Lurasidone 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 Lurasidone manufacturer or Lurasidone supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lurasidone manufacturer or Lurasidone supplier.
PharmaCompass also assists you with knowing the Lurasidone API Price utilized in the formulation of products. Lurasidone API Price is not always fixed or binding as the Lurasidone Price is obtained through a variety of data sources. The Lurasidone Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A latuda manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of latuda, including repackagers and relabelers. The FDA regulates latuda manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. latuda 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 latuda manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A latuda supplier is an individual or a company that provides latuda active pharmaceutical ingredient (API) or latuda finished formulations upon request. The latuda suppliers may include latuda API manufacturers, exporters, distributors and traders.
click here to find a list of latuda 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 latuda Drug Master File in Japan (latuda JDMF) empowers latuda 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 latuda JDMF during the approval evaluation for pharmaceutical products. At the time of latuda 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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