01 1Divi’s Laboratories
02 1M/s Divis Laboratories
01 1Iopromide EP
02 1Iopromide Ph.Eur
01 1WC-0031
02 1WC-0031A3
01 2India
Date of Issue : 2022-06-16
Valid Till : 2025-06-16
Written Confirmation Number : WC-0031
Address of the Firm : Unit-Lingojigudem (V) Choutuppal (M) Nalgonda District Talangana State India
Date of Issue : 2020-12-18
Valid Till : 2022-06-16
Written Confirmation Number : WC-0031A3
Address of the Firm : Unit-Lingojigudem (V) Choutuppal (M) Nalgonda District Talangana State India
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PharmaCompass offers a list of Iopromide 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 Iopromide manufacturer or Iopromide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iopromide manufacturer or Iopromide supplier.
PharmaCompass also assists you with knowing the Iopromide API Price utilized in the formulation of products. Iopromide API Price is not always fixed or binding as the Iopromide Price is obtained through a variety of data sources. The Iopromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ultravist 370 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ultravist 370, including repackagers and relabelers. The FDA regulates Ultravist 370 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ultravist 370 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 Ultravist 370 supplier is an individual or a company that provides Ultravist 370 active pharmaceutical ingredient (API) or Ultravist 370 finished formulations upon request. The Ultravist 370 suppliers may include Ultravist 370 API manufacturers, exporters, distributors and traders.
click here to find a list of Ultravist 370 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Ultravist 370 written confirmation (Ultravist 370 WC) is an official document issued by a regulatory agency to a Ultravist 370 manufacturer, verifying that the manufacturing facility of a Ultravist 370 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ultravist 370 APIs or Ultravist 370 finished pharmaceutical products to another nation, regulatory agencies frequently require a Ultravist 370 WC (written confirmation) as part of the regulatory process.
click here to find a list of Ultravist 370 suppliers with Written Confirmation (WC) on PharmaCompass.
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