01 1Ajinomoto Co., Inc.
01 1Arginine Monohydrochloride
01 1Japan
NDC Package Code : 17333-004
Start Marketing Date : 2002-06-28
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 L-Arginine Hydrochloride API 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 L-Arginine Hydrochloride API manufacturer or L-Arginine Hydrochloride API supplier for your needs.
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PharmaCompass also assists you with knowing the L-Arginine Hydrochloride API API Price utilized in the formulation of products. L-Arginine Hydrochloride API API Price is not always fixed or binding as the L-Arginine Hydrochloride API Price is obtained through a variety of data sources. The L-Arginine Hydrochloride API Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A R-gene 10 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of R-gene 10, including repackagers and relabelers. The FDA regulates R-gene 10 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. R-gene 10 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 R-gene 10 supplier is an individual or a company that provides R-gene 10 active pharmaceutical ingredient (API) or R-gene 10 finished formulations upon request. The R-gene 10 suppliers may include R-gene 10 API manufacturers, exporters, distributors and traders.
click here to find a list of R-gene 10 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 R-gene 10 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for R-gene 10 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 R-gene 10 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 R-gene 10 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a R-gene 10 NDC to their finished compounded human drug products, they may choose to do so.
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