01 1AAA Molybdenum Products Inc
01 1Ammonium Tetrathiomolybdate
01 1U.S.A
NDC Package Code : 82680-001
Start Marketing Date : 2022-04-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25g/25g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Ammonium Tetrathiomolybdate 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 Ammonium Tetrathiomolybdate manufacturer or Ammonium Tetrathiomolybdate supplier for your needs.
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PharmaCompass also assists you with knowing the Ammonium Tetrathiomolybdate API Price utilized in the formulation of products. Ammonium Tetrathiomolybdate API Price is not always fixed or binding as the Ammonium Tetrathiomolybdate Price is obtained through a variety of data sources. The Ammonium Tetrathiomolybdate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tiomolibdate diammonium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tiomolibdate diammonium, including repackagers and relabelers. The FDA regulates Tiomolibdate diammonium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tiomolibdate diammonium 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 Tiomolibdate diammonium supplier is an individual or a company that provides Tiomolibdate diammonium active pharmaceutical ingredient (API) or Tiomolibdate diammonium finished formulations upon request. The Tiomolibdate diammonium suppliers may include Tiomolibdate diammonium API manufacturers, exporters, distributors and traders.
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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 Tiomolibdate diammonium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tiomolibdate diammonium 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 Tiomolibdate diammonium 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 Tiomolibdate diammonium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tiomolibdate diammonium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tiomolibdate diammonium suppliers with NDC on PharmaCompass.
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