01 1Glaxo Operations UK Limited
02 1Piramal Pharma Limited
03 1Thermo Fisher Scientific Cork Limited
01 3GlaxoSmithKline Inc.
01 3Abacavir sulfate
01 1India
02 1U.S.A
03 1United Kingdom
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2009-11-12
Registration Number : 89-7-ND
Manufacturer Name : Glaxo Operations UK Limited
Manufacturer Address : Cobden Street, Montrose, Angus, DD10 8EA
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2010-04-22
Registration Number : 89-9-ND
Manufacturer Name : Piramal Pharma Limited
Manufacturer Address : Sy. Nos. 7-70, 70/1 and 70/2, Digwal Village, Kohir Mandal, Sangareddy District, Tela...
Registrant Name : GlaxoSmithKline Inc.
Registration Date : 2009-11-12
Registration Number : 89-8-ND
Manufacturer Name : Thermo Fisher Scientific Cor...
Manufacturer Address : Currabinny, Carrigaline, County Cork, P43 AY66, Ireland
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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, and more, enabling you to easily find the right Abacavir Sulfate manufacturer or Abacavir Sulfate supplier for your needs.
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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, and COA 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, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a TRIZIVIR Drug Master File in Korea (TRIZIVIR KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of TRIZIVIR. The MFDS reviews the TRIZIVIR KDMF as part of the drug registration process and uses the information provided in the TRIZIVIR KDMF to evaluate the safety and efficacy of the drug.
After submitting a TRIZIVIR KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their TRIZIVIR API can apply through the Korea Drug Master File (KDMF).
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