01 1Changzhou Tianhua Pharmaceutical Co., Ltd.
02 1Fagron Inc
03 1LETCO MEDICAL, LLC
04 1Professional Compounding Centers of America
05 1Yumen Qianhua Pharmaceutical Co., Ltd.
01 2DYCLONINE HYDROCHLORIDE
02 1Dyclonine HCl
03 2Dyclonine Hydrochloride
01 1China
02 1Netherlands
03 1U.S.A
04 1United Kingdom
05 1Blank
NDC Package Code : 66219-0006
Start Marketing Date : 2015-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1037
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-06-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-1661
Start Marketing Date : 2009-05-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0227
Start Marketing Date : 2022-02-02
End Marketing Date : 2025-06-15
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 84317-103
Start Marketing Date : 2024-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A dyclonine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of dyclonine hydrochloride, including repackagers and relabelers. The FDA regulates dyclonine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. dyclonine 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 dyclonine hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A dyclonine hydrochloride supplier is an individual or a company that provides dyclonine hydrochloride active pharmaceutical ingredient (API) or dyclonine hydrochloride finished formulations upon request. The dyclonine hydrochloride suppliers may include dyclonine hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of dyclonine 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 dyclonine hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for dyclonine 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 dyclonine 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 dyclonine hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a dyclonine hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of dyclonine hydrochloride suppliers with NDC on PharmaCompass.
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