01 1QINGDAO TIDA BIOTEK CO.,LTD
01 1L-Citrulline
01 1China
NDC Package Code : 90027-027
Start Marketing Date : 2023-08-16
End Marketing Date : 2026-03-27
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Citrulline 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 Citrulline manufacturer or Citrulline supplier for your needs.
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PharmaCompass also assists you with knowing the Citrulline API Price utilized in the formulation of products. Citrulline API Price is not always fixed or binding as the Citrulline Price is obtained through a variety of data sources. The Citrulline Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EINECS 206-759-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EINECS 206-759-6, including repackagers and relabelers. The FDA regulates EINECS 206-759-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EINECS 206-759-6 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 EINECS 206-759-6 supplier is an individual or a company that provides EINECS 206-759-6 active pharmaceutical ingredient (API) or EINECS 206-759-6 finished formulations upon request. The EINECS 206-759-6 suppliers may include EINECS 206-759-6 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 EINECS 206-759-6 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for EINECS 206-759-6 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 EINECS 206-759-6 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 EINECS 206-759-6 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a EINECS 206-759-6 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of EINECS 206-759-6 suppliers with NDC on PharmaCompass.
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