01 1Honor Lab Limited
01 1Alogliptin benzoate “D”
01 1India
Registration Number : 306MF10015
Registrant's Address : H. No. &8-3-166/7/1, Erragadda, Hyderabad-500018, Telangana, INDIA.
Initial Date of Registration : 2024-01-24
Latest Date of Registration : 2024-01-24
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PharmaCompass offers a list of Alogliptin Benzoate 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 Alogliptin Benzoate manufacturer or Alogliptin Benzoate supplier for your needs.
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PharmaCompass also assists you with knowing the Alogliptin Benzoate API Price utilized in the formulation of products. Alogliptin Benzoate API Price is not always fixed or binding as the Alogliptin Benzoate Price is obtained through a variety of data sources. The Alogliptin Benzoate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A nesina manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of nesina, including repackagers and relabelers. The FDA regulates nesina manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. nesina API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A nesina supplier is an individual or a company that provides nesina active pharmaceutical ingredient (API) or nesina finished formulations upon request. The nesina suppliers may include nesina API manufacturers, exporters, distributors and traders.
click here to find a list of nesina 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 nesina Drug Master File in Japan (nesina JDMF) empowers nesina 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 nesina JDMF during the approval evaluation for pharmaceutical products. At the time of nesina 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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