01 1Curia Spain S.A.U.
02 1Henan Lihua Pharmaceutical Co Ltd
03 1NEWCHEM SPA
04 1Symbiotica Speciality Ingredients Sdn. Bhd.
05 1Taisho Pharmaceutical Co., Ltd.
01 2Hydrocortisone Butyrate
02 1Hydrocortisone Butyrate Micronized
03 1Hydrocortisone butyrate
04 1Hydrocortisone probutate
01 1China
02 1Italy
03 1Japan
04 1Malaysia
05 1U.S.A
NDC Package Code : 65089-0035
Start Marketing Date : 1982-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64958-0030
Start Marketing Date : 2006-08-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24002-0017
Start Marketing Date : 2009-07-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52128-130
Start Marketing Date : 2004-06-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48246-100
Start Marketing Date : 1996-08-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (2kg/2kg)
Marketing Category : BULK INGREDIENT
A Hydrocortisone Butyrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Butyrate, including repackagers and relabelers. The FDA regulates Hydrocortisone Butyrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Butyrate 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 Butyrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Butyrate supplier is an individual or a company that provides Hydrocortisone Butyrate active pharmaceutical ingredient (API) or Hydrocortisone Butyrate finished formulations upon request. The Hydrocortisone Butyrate suppliers may include Hydrocortisone Butyrate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Butyrate 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 Butyrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydrocortisone Butyrate 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 Butyrate 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 Butyrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydrocortisone Butyrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydrocortisone Butyrate suppliers with NDC on PharmaCompass.
We have 5 companies offering Hydrocortisone Butyrate
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