01 2M/s Zydus Takeda Healthcare Pvt ltd
01 1Podophyllotoxin IH
02 1Podophyllotoxin Ph.Eur.
01 2WC-0204
01 2India
Date of Issue : 2022-06-15
Valid Till : 2025-07-07
Written Confirmation Number : WC-0204
Address of the Firm : C-4, MIDC, Village Pawne, Thane Belapur Road, Vashi, Navi Mumbai ? 400 703
Date of Issue : 2022-06-15
Valid Till : 2025-07-07
Written Confirmation Number : WC-0204
Address of the Firm : C-4, MIDC, Village Pawne, Thane Belapur Road, Vashi, Navi Mumbai ? 400 703
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PharmaCompass offers a list of Podophyllotoxin 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 Podophyllotoxin manufacturer or Podophyllotoxin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Podophyllotoxin manufacturer or Podophyllotoxin supplier.
PharmaCompass also assists you with knowing the Podophyllotoxin API Price utilized in the formulation of products. Podophyllotoxin API Price is not always fixed or binding as the Podophyllotoxin Price is obtained through a variety of data sources. The Podophyllotoxin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tox21_202922 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_202922, including repackagers and relabelers. The FDA regulates Tox21_202922 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_202922 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_202922 supplier is an individual or a company that provides Tox21_202922 active pharmaceutical ingredient (API) or Tox21_202922 finished formulations upon request. The Tox21_202922 suppliers may include Tox21_202922 API manufacturers, exporters, distributors and traders.
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A Tox21_202922 written confirmation (Tox21_202922 WC) is an official document issued by a regulatory agency to a Tox21_202922 manufacturer, verifying that the manufacturing facility of a Tox21_202922 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tox21_202922 APIs or Tox21_202922 finished pharmaceutical products to another nation, regulatory agencies frequently require a Tox21_202922 WC (written confirmation) as part of the regulatory process.
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