01 1Biovet Joint Stock Company
01 1Monensin
01 1Blank
NDC Package Code : 11311-971
Start Marketing Date : 2011-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Monensin 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 Monensin Sodium manufacturer or Monensin Sodium supplier for your needs.
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PharmaCompass also assists you with knowing the Monensin Sodium API Price utilized in the formulation of products. Monensin Sodium API Price is not always fixed or binding as the Monensin Sodium Price is obtained through a variety of data sources. The Monensin Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Monensin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Monensin Sodium, including repackagers and relabelers. The FDA regulates Monensin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Monensin 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 Monensin Sodium supplier is an individual or a company that provides Monensin Sodium active pharmaceutical ingredient (API) or Monensin Sodium finished formulations upon request. The Monensin Sodium suppliers may include Monensin Sodium 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 Monensin Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Monensin 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 Monensin 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 Monensin Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Monensin Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Monensin Sodium suppliers with NDC on PharmaCompass.
