Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
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01 1Syn-Tech Chem & Pharm Co., Ltd.
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01 1Orciprenaline Sulfate
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01 1TFDA-0002291
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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
82
PharmaCompass offers a list of Metaproterenol Hemisulfate 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 Metaproterenol Hemisulfate manufacturer or Metaproterenol Hemisulfate supplier for your needs.
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PharmaCompass also assists you with knowing the Metaproterenol Hemisulfate API Price utilized in the formulation of products. Metaproterenol Hemisulfate API Price is not always fixed or binding as the Metaproterenol Hemisulfate Price is obtained through a variety of data sources. The Metaproterenol Hemisulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Alupent manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alupent, including repackagers and relabelers. The FDA regulates Alupent manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alupent 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 Alupent supplier is an individual or a company that provides Alupent active pharmaceutical ingredient (API) or Alupent finished formulations upon request. The Alupent suppliers may include Alupent API manufacturers, exporters, distributors and traders.
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A Alupent written confirmation (Alupent WC) is an official document issued by a regulatory agency to a Alupent manufacturer, verifying that the manufacturing facility of a Alupent active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Alupent APIs or Alupent finished pharmaceutical products to another nation, regulatory agencies frequently require a Alupent WC (written confirmation) as part of the regulatory process.
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