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 Hydrochloride 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 Hydrochloride manufacturer or Lurasidone Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Lurasidone Hydrochloride API Price utilized in the formulation of products. Lurasidone Hydrochloride API Price is not always fixed or binding as the Lurasidone Hydrochloride Price is obtained through a variety of data sources. The Lurasidone Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A SMP-13496 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SMP-13496, including repackagers and relabelers. The FDA regulates SMP-13496 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SMP-13496 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 SMP-13496 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SMP-13496 supplier is an individual or a company that provides SMP-13496 active pharmaceutical ingredient (API) or SMP-13496 finished formulations upon request. The SMP-13496 suppliers may include SMP-13496 API manufacturers, exporters, distributors and traders.
click here to find a list of SMP-13496 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 SMP-13496 Drug Master File in Japan (SMP-13496 JDMF) empowers SMP-13496 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 SMP-13496 JDMF during the approval evaluation for pharmaceutical products. At the time of SMP-13496 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 SMP-13496 suppliers with JDMF on PharmaCompass.
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