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.
02 1M/s Bioxera Pharma Pvt Ltd
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01 1Pramoxine Hydrochloride
02 1Pramoxine Hydrochloride USP
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01 1TFDA-0002291
02 1WC-0248
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01 1India
02 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
Date of Issue : 2022-09-07
Valid Till : 2025-07-02
Written Confirmation Number : WC-0248
Address of the Firm : Plot No. N-57, Anand Nagar, Additional M.I.D.C., Ambernath (East)-421506, Mahara...

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PharmaCompass offers a list of Pramoxine Hydrochloride 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 Pramoxine Hydrochloride manufacturer or Pramoxine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pramoxine Hydrochloride manufacturer or Pramoxine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Pramoxine Hydrochloride API Price utilized in the formulation of products. Pramoxine Hydrochloride API Price is not always fixed or binding as the Pramoxine Hydrochloride Price is obtained through a variety of data sources. The Pramoxine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A KM0782 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KM0782, including repackagers and relabelers. The FDA regulates KM0782 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KM0782 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of KM0782 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A KM0782 supplier is an individual or a company that provides KM0782 active pharmaceutical ingredient (API) or KM0782 finished formulations upon request. The KM0782 suppliers may include KM0782 API manufacturers, exporters, distributors and traders.
click here to find a list of KM0782 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A KM0782 written confirmation (KM0782 WC) is an official document issued by a regulatory agency to a KM0782 manufacturer, verifying that the manufacturing facility of a KM0782 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting KM0782 APIs or KM0782 finished pharmaceutical products to another nation, regulatory agencies frequently require a KM0782 WC (written confirmation) as part of the regulatory process.
click here to find a list of KM0782 suppliers with Written Confirmation (WC) on PharmaCompass.
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