01 1Ajinomoto Co., Inc.
02 1KYOWA HAKKO BIO CO., LTD.
03 1Taenaka Kogyo Co., Ltd.
04 1Willow Birch Pharma, Inc
01 1L-Cysteine Hydrochloide Monohydrate
02 2L-Cysteine Hydrochloride Monohydrate
03 1L-Cysteine Monohydrochloride Monohydrate
01 3Japan
02 1U.S.A
NDC Package Code : 17333-909
Start Marketing Date : 2008-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12497-1013
Start Marketing Date : 1978-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 53884-1013
Start Marketing Date : 2023-01-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 10695-128
Start Marketing Date : 2024-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A L-Cysteine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of L-Cysteine Hydrochloride, including repackagers and relabelers. The FDA regulates L-Cysteine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. L-Cysteine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of L-Cysteine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A L-Cysteine Hydrochloride supplier is an individual or a company that provides L-Cysteine Hydrochloride active pharmaceutical ingredient (API) or L-Cysteine Hydrochloride finished formulations upon request. The L-Cysteine Hydrochloride suppliers may include L-Cysteine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of L-Cysteine Hydrochloride 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 L-Cysteine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for L-Cysteine Hydrochloride 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 L-Cysteine Hydrochloride 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 L-Cysteine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a L-Cysteine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of L-Cysteine Hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering L-Cysteine Hydrochloride
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