01 1Genentech, Inc.
01 1ganciclovir sodium
01 1U.S.A
NDC Package Code : 0004-6941
Start Marketing Date : 1989-06-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (500mg/.01kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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PharmaCompass offers a list of Ganciclovir Sodium 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 Ganciclovir Sodium manufacturer or Ganciclovir Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Ganciclovir Sodium API Price utilized in the formulation of products. Ganciclovir Sodium API Price is not always fixed or binding as the Ganciclovir Sodium Price is obtained through a variety of data sources. The Ganciclovir Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ganciclovir Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ganciclovir Sodium, including repackagers and relabelers. The FDA regulates Ganciclovir Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ganciclovir Sodium 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 Ganciclovir Sodium supplier is an individual or a company that provides Ganciclovir Sodium active pharmaceutical ingredient (API) or Ganciclovir Sodium finished formulations upon request. The Ganciclovir Sodium suppliers may include Ganciclovir Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Ganciclovir Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Ganciclovir Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ganciclovir Sodium API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Ganciclovir Sodium as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Ganciclovir Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ganciclovir Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ganciclovir Sodium suppliers with NDC on PharmaCompass.
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