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01 1Hetero Labs Limited
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01 1Lamivudine
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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 (+/-)-3TC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+/-)-3TC, including repackagers and relabelers. The FDA regulates (+/-)-3TC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+/-)-3TC 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 (+/-)-3TC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+/-)-3TC supplier is an individual or a company that provides (+/-)-3TC active pharmaceutical ingredient (API) or (+/-)-3TC finished formulations upon request. The (+/-)-3TC suppliers may include (+/-)-3TC API manufacturers, exporters, distributors and traders.
click here to find a list of (+/-)-3TC 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 (+/-)-3TC Drug Master File in Japan ((+/-)-3TC JDMF) empowers (+/-)-3TC 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 (+/-)-3TC JDMF during the approval evaluation for pharmaceutical products. At the time of (+/-)-3TC 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 (+/-)-3TC suppliers with JDMF on PharmaCompass.
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