Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
01 1Syn-Tech Chem & Pharm Co., Ltd.
01 1Oxazolam
01 1TFDA-0002291
01 1Taiwan
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Date of Issue : 2022-02-22
Valid Till : 2025-07-15
Written Confirmation Number : TFDA-0002291
Address of the Firm : No. 168, Kai Yuan Rd, Hsin-Ying, Tainan City 73055, Taiwan
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PharmaCompass offers a list of Oxazolam 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 Oxazolam manufacturer or Oxazolam supplier for your needs.
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PharmaCompass also assists you with knowing the Oxazolam API Price utilized in the formulation of products. Oxazolam API Price is not always fixed or binding as the Oxazolam Price is obtained through a variety of data sources. The Oxazolam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tranquit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tranquit, including repackagers and relabelers. The FDA regulates Tranquit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tranquit API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Tranquit supplier is an individual or a company that provides Tranquit active pharmaceutical ingredient (API) or Tranquit finished formulations upon request. The Tranquit suppliers may include Tranquit API manufacturers, exporters, distributors and traders.
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A Tranquit written confirmation (Tranquit WC) is an official document issued by a regulatory agency to a Tranquit manufacturer, verifying that the manufacturing facility of a Tranquit active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Tranquit APIs or Tranquit finished pharmaceutical products to another nation, regulatory agencies frequently require a Tranquit WC (written confirmation) as part of the regulatory process.
click here to find a list of Tranquit suppliers with Written Confirmation (WC) on PharmaCompass.
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