01 M/s Hetero Drugs Limited (1)
02 M/s. Aurobindo Pharma Ltd., (Unit-XI), (1)
03 M/s. Aurobindo Pharma Ltd., (1)
04 M/s. Cipla Limited, (1)
05 M/s. Hetero Labs Limited., (1)
06 M/s. Hetro Labs Limited (1)
07 M/s. Mylan Laboratories Ltd., (2)
01 Zidovudine (Ph. Eur.) (1)
02 Zidovudine (Ph.Eur) (2)
03 Zidovudine (Ph.Eur.) (1)
04 Zidovudine (USP/Ph. Eur) (1)
05 Zidovudine (USP/Ph. Eur.) (1)
06 Zidovudine USP/EP (1)
07 Zidovudine Ph. Eur./USP/IP (1)
01 WC-0016 (1)
02 WC-0017 (1)
03 WC-0023 (1)
04 WC-0041 (1)
05 WC-0065 (1)
06 WC-0065a (1)
07 WC-0113 (1)
08 WC-0118 (1)
01 India (8)
57
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PharmaCompass also assists you with knowing the Zidovudine API Price utilized in the formulation of products. Zidovudine API Price is not always fixed or binding as the Zidovudine Price is obtained through a variety of data sources. The Zidovudine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_300578 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300578, including repackagers and relabelers. The FDA regulates Tox21_300578 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300578 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 Tox21_300578 supplier is an individual or a company that provides Tox21_300578 active pharmaceutical ingredient (API) or Tox21_300578 finished formulations upon request. The Tox21_300578 suppliers may include Tox21_300578 API manufacturers, exporters, distributors and traders.
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A Tox21_300578 written confirmation (Tox21_300578 WC) is an official document issued by a regulatory agency to a Tox21_300578 manufacturer, verifying that the manufacturing facility of a Tox21_300578 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tox21_300578 APIs or Tox21_300578 finished pharmaceutical products to another nation, regulatory agencies frequently require a Tox21_300578 WC (written confirmation) as part of the regulatory process.
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We have 4 companies offering Tox21_300578
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