01 1Kumar Organic Products Limited
01 1Triclosan
01 1India
NDC Package Code : 63934-110
Start Marketing Date : 2000-01-01
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 Triclosan 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 Triclosan manufacturer or Triclosan supplier for your needs.
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A Ster Zac Bath Concentrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ster Zac Bath Concentrate, including repackagers and relabelers. The FDA regulates Ster Zac Bath Concentrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ster Zac Bath Concentrate 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 Ster Zac Bath Concentrate supplier is an individual or a company that provides Ster Zac Bath Concentrate active pharmaceutical ingredient (API) or Ster Zac Bath Concentrate finished formulations upon request. The Ster Zac Bath Concentrate suppliers may include Ster Zac Bath Concentrate 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 Ster Zac Bath Concentrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ster Zac Bath Concentrate 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 Ster Zac Bath Concentrate 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 Ster Zac Bath Concentrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ster Zac Bath Concentrate NDC to their finished compounded human drug products, they may choose to do so.
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