01 1Hetero Labs Limited
01 1Lamivudine
01 1India
Registration Number : 229MF10157
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2017-08-08
Latest Date of Registration : 2020-05-12
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PharmaCompass offers a list of Lamivudine 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 Lamivudine manufacturer or Lamivudine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lamivudine manufacturer or Lamivudine supplier.
PharmaCompass also assists you with knowing the Lamivudine API Price utilized in the formulation of products. Lamivudine API Price is not always fixed or binding as the Lamivudine Price is obtained through a variety of data sources. The Lamivudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A LMV manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LMV, including repackagers and relabelers. The FDA regulates LMV manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LMV 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 LMV manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LMV supplier is an individual or a company that provides LMV active pharmaceutical ingredient (API) or LMV finished formulations upon request. The LMV suppliers may include LMV API manufacturers, exporters, distributors and traders.
click here to find a list of LMV 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 LMV Drug Master File in Japan (LMV JDMF) empowers LMV 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 LMV JDMF during the approval evaluation for pharmaceutical products. At the time of LMV 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 LMV suppliers with JDMF on PharmaCompass.
