01 M/s. Piramal Enterprises Limited (1)
02 M/s Hetero Drugs Limited (1)
03 M/s Mylan Laboratories Limited (1)
04 M/s mylan laboratories Limited (1)
05 M/s. Aurobindo Pharma Ltd., (Unit-XI), (1)
06 M/s. Cipla Ltd. (1)
07 M/s. Hetero Labs Limited., (1)
08 M/s. Hetro Labs Limited (1)
09 M/s. Laurus Labs Pvt. Ltd., (1)
10 M/s. Lupin Ltd (1)
11 M/s. Mylan Laboratories Ltd., (1)
12 M/s.Granules India (1)
01 Abacavir Sulfate (USP) (2)
02 Abacavir Sulfate (USP)/ Abacavir Hydrochloride IH (1)
03 Abacavir Sulfate (USP/IH/Ph. Eur/Ph. Int) (1)
04 Abacavir Sulfate Ph.Eur (1)
05 Abacavir Sulfate USP/EP (1)
06 Abacavir Sulphate (Ph. Eur.) (1)
07 Abacavir Sulphate (USP) (1)
08 Abacavir Sulphate EP (2)
09 Abacavir Sulphate USP (2)
01 WC-0015 (1)
02 WC-0023 (1)
03 WC-0024 (1)
04 WC-0041 (1)
05 WC-0065 (1)
06 WC-0065a (1)
07 WC-0123 (1)
08 WC-0140 (1)
09 WC-0201 (1)
10 WC-0213 (1)
11 WC-0359 (1)
12 WC-0359a3 (1)
01 India (12)
50
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.
click here to find a list of TRIZIVIR manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
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.
A TRIZIVIR written confirmation (TRIZIVIR WC) is an official document issued by a regulatory agency to a TRIZIVIR manufacturer, verifying that the manufacturing facility of a TRIZIVIR active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting TRIZIVIR APIs or TRIZIVIR finished pharmaceutical products to another nation, regulatory agencies frequently require a TRIZIVIR WC (written confirmation) as part of the regulatory process.
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