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
A Lurasidone HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lurasidone HCl, including repackagers and relabelers. The FDA regulates Lurasidone HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lurasidone HCl 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 Lurasidone HCl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lurasidone HCl supplier is an individual or a company that provides Lurasidone HCl active pharmaceutical ingredient (API) or Lurasidone HCl finished formulations upon request. The Lurasidone HCl suppliers may include Lurasidone HCl API manufacturers, exporters, distributors and traders.
click here to find a list of Lurasidone HCl 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 Lurasidone HCl Drug Master File in Japan (Lurasidone HCl JDMF) empowers Lurasidone HCl 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 Lurasidone HCl JDMF during the approval evaluation for pharmaceutical products. At the time of Lurasidone HCl 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 Lurasidone HCl suppliers with JDMF on PharmaCompass.
We have 1 companies offering Lurasidone HCl
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
