01 1Curium US LLC
01 1OXIDRONATE SODIUM
01 1U.S.A
NDC Package Code : 69945-410
Start Marketing Date : 2016-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Disodium Methanehydroxydiphosphonate 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 Disodium Methanehydroxydiphosphonate manufacturer or Disodium Methanehydroxydiphosphonate supplier for your needs.
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PharmaCompass also assists you with knowing the Disodium Methanehydroxydiphosphonate API Price utilized in the formulation of products. Disodium Methanehydroxydiphosphonate API Price is not always fixed or binding as the Disodium Methanehydroxydiphosphonate Price is obtained through a variety of data sources. The Disodium Methanehydroxydiphosphonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Oxidronate disodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxidronate disodium, including repackagers and relabelers. The FDA regulates Oxidronate disodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxidronate disodium 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 Oxidronate disodium supplier is an individual or a company that provides Oxidronate disodium active pharmaceutical ingredient (API) or Oxidronate disodium finished formulations upon request. The Oxidronate disodium suppliers may include Oxidronate disodium API manufacturers, exporters, distributors and traders.
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 Oxidronate disodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Oxidronate disodium 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 Oxidronate disodium 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 Oxidronate disodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Oxidronate disodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Oxidronate disodium suppliers with NDC on PharmaCompass.
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