01 M/s Azico Biophore India (1)
02 M/s Azico Biophore India Pvt Ltd (1)
03 M/s Danashmand Organics Pvt Ltd (1)
04 M/s. Srikem Laboratories P (LTD) (1)
01 Permethrin (IH)/EP (1)
02 Permethrin (Ph. Eur/HIS) (1)
03 Permethrin BP/EP (1)
04 Permethrin IH/EP (1)
01 WC-0404 (1)
02 WC-0404A2 (1)
03 WC-0415 (1)
04 WC-246 (1)
01 India (4)
24
PharmaCompass offers a list of Permethrin 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 Permethrin manufacturer or Permethrin supplier for your needs.
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A Tox21_300691 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300691, including repackagers and relabelers. The FDA regulates Tox21_300691 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300691 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_300691 supplier is an individual or a company that provides Tox21_300691 active pharmaceutical ingredient (API) or Tox21_300691 finished formulations upon request. The Tox21_300691 suppliers may include Tox21_300691 API manufacturers, exporters, distributors and traders.
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A Tox21_300691 written confirmation (Tox21_300691 WC) is an official document issued by a regulatory agency to a Tox21_300691 manufacturer, verifying that the manufacturing facility of a Tox21_300691 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tox21_300691 APIs or Tox21_300691 finished pharmaceutical products to another nation, regulatory agencies frequently require a Tox21_300691 WC (written confirmation) as part of the regulatory process.
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