ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
01 1ICE SpA
02 1Arch Pharmalabs Limited
03 1Daewoong Bio Inc.
04 1Daewoong Bio Inc._3rd Plant
05 1Darmerica, LLC
06 4Dipharma Francis Srl
07 1Fagron Inc
08 1Glenmark Life Sciences Limited
09 1Kalchem International inc
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 1Professional Compounding Centers of America dba PCCA
13 1Sichuan Huigukang Biological Technology Co., Ltd.
14 1Sichuan Xieli Pharmaceutical Co., Ltd.
15 1Spectrum Laboratory Products, Inc.
01 3URSODIOL
02 1URSODIOL (Process II)
03 2Ursodeoxycholic Acid
04 10Ursodiol
05 1Ursodiol (Process IV)
06 1ursodiol
01 2China
02 2India
03 5Italy
04 1Netherlands
05 2South Korea
06 5U.S.A
07 1United Kingdom
ICE Pharma offers a unique range of bile acid products and best-in-class services for the pharmaceutical industry.
NDC Package Code : 49345-2612
Start Marketing Date : 2002-05-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22365-012
Start Marketing Date : 2018-12-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0089
Start Marketing Date : 1994-10-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0090
Start Marketing Date : 2005-11-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0653
Start Marketing Date : 2018-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0654
Start Marketing Date : 2005-11-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0906
Start Marketing Date : 2004-09-01
End Marketing Date : 2027-07-11
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-1987
Start Marketing Date : 2014-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2909
Start Marketing Date : 1999-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-8085
Start Marketing Date : 2000-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Ursodiol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ursodiol, including repackagers and relabelers. The FDA regulates Ursodiol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ursodiol 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 Ursodiol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ursodiol supplier is an individual or a company that provides Ursodiol active pharmaceutical ingredient (API) or Ursodiol finished formulations upon request. The Ursodiol suppliers may include Ursodiol API manufacturers, exporters, distributors and traders.
click here to find a list of Ursodiol 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 Ursodiol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ursodiol 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 Ursodiol 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 Ursodiol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ursodiol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ursodiol suppliers with NDC on PharmaCompass.
We have 15 companies offering Ursodiol
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