01 1LUPIN LIMITED.
01 1Abacavir sulfate
01 1India
Registration Number : 229MF10171
Registrant's Address : Kalpataru Inspire, 3rd Floor, Off Western Express Highway, Santacruz (East), Mumbai 4...
Initial Date of Registration : 2017-08-28
Latest Date of Registration : 2020-08-18
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PharmaCompass offers a list of Abacavir Sulfate 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 Abacavir Sulfate manufacturer or Abacavir Sulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Abacavir Sulfate API Price utilized in the formulation of products. Abacavir Sulfate API Price is not always fixed or binding as the Abacavir Sulfate Price is obtained through a variety of data sources. The Abacavir Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A TRIZIVIR manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of TRIZIVIR, including repackagers and relabelers. The FDA regulates TRIZIVIR manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. TRIZIVIR 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 TRIZIVIR supplier is an individual or a company that provides TRIZIVIR active pharmaceutical ingredient (API) or TRIZIVIR finished formulations upon request. The TRIZIVIR suppliers may include TRIZIVIR API manufacturers, exporters, distributors and traders.
click here to find a list of TRIZIVIR 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 TRIZIVIR Drug Master File in Japan (TRIZIVIR JDMF) empowers TRIZIVIR 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 TRIZIVIR JDMF during the approval evaluation for pharmaceutical products. At the time of TRIZIVIR 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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