EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 2EUROAPI FRANCE
02 1HENAN LIHUA PHARMACEUTICAL CO., LTD
03 1Symbiotica Speciality Ingredients Sdn. Bhd.
04 1Trifarma S.p.A
01 5Hydrocortisone Valerate
01 1China
02 2France
03 1Italy
04 1Malaysia
NDC Package Code : 82298-115
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82298-116
Start Marketing Date : 2011-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64958-0080
Start Marketing Date : 2001-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52128-136
Start Marketing Date : 2007-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46204-0689
Start Marketing Date : 2016-11-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Hydrocortisone Valerate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Valerate, including repackagers and relabelers. The FDA regulates Hydrocortisone Valerate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Valerate 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 Hydrocortisone Valerate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Valerate supplier is an individual or a company that provides Hydrocortisone Valerate active pharmaceutical ingredient (API) or Hydrocortisone Valerate finished formulations upon request. The Hydrocortisone Valerate suppliers may include Hydrocortisone Valerate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Valerate 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 Hydrocortisone Valerate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydrocortisone Valerate 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 Hydrocortisone Valerate 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 Hydrocortisone Valerate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydrocortisone Valerate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydrocortisone Valerate suppliers with NDC on PharmaCompass.
We have 4 companies offering Hydrocortisone Valerate
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