Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
02 1HENANA LIHUA PHARMACEUTICALS CO., INC.
03 2Henan Lihua Pharmaceutical Co Ltd
04 1Isomedix Operations
05 1Isomedix Operations, Inc
06 1Jiangsu Jiaerke Pharmaceuticals Group Corp., Ltd.
07 1Jiangsu Lianhuan Pharmaceutical Co., Ltd
08 1Medisca Inc.
09 1Newchem SpA
10 1Pharmacia and Upjohn Company LLC
11 1Professional Compounding Centers of America
12 1Professional Compounding Centers of America dba PCCA
13 1Shandong Xinhua Pharmaceutical Co., Ltd.
14 3Shandong Xinhua Pharmaceutical Company Limited
15 1Spectrum Laboratory Products, Inc.
16 1Tianjin Jinjin Pharmaceutical Co., Ltd.
17 1Zhejiang Xianju Pharmaceutical Co., Ltd.
01 5HYDROCORTISONE ACETATE
02 12Hydrocortisone Acetate
03 1Hydrocortisone acetate
04 1Hydrocotisone Acetate
05 1hydrocortisone acetate
01 11China
02 1India
03 1Italy
04 4U.S.A
05 2United Kingdom
06 1Blank
NDC Package Code : 22552-0036
Start Marketing Date : 2013-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0008
Start Marketing Date : 2011-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24002-0035
Start Marketing Date : 2020-09-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0196
Start Marketing Date : 2004-09-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1110
Start Marketing Date : 2013-06-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-5161
Start Marketing Date : 2014-07-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58624-0704
Start Marketing Date : 1984-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3590
Start Marketing Date : 1989-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55718-164
Start Marketing Date : 2023-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 55718-172
Start Marketing Date : 2015-01-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10mg/g)
Marketing Category : DRUG FOR FURTHER PROCESSING
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A Hydrocortisone Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydrocortisone Acetate, including repackagers and relabelers. The FDA regulates Hydrocortisone Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydrocortisone Acetate 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 Acetate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydrocortisone Acetate supplier is an individual or a company that provides Hydrocortisone Acetate active pharmaceutical ingredient (API) or Hydrocortisone Acetate finished formulations upon request. The Hydrocortisone Acetate suppliers may include Hydrocortisone Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Hydrocortisone Acetate 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 Acetate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydrocortisone Acetate 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 Acetate 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 Acetate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydrocortisone Acetate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydrocortisone Acetate suppliers with NDC on PharmaCompass.
We have 13 companies offering Hydrocortisone Acetate
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