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01 1Fermion Oy
02 1Fine Chemicals Corporation (PTY) Ltd.
03 1Aarti Pharmalabs Limited
04 1APICHEM Laboratories Private Limited
05 1Apicore Pharmaceuticals Private Limited
06 1Excella GmbH & Co. KG
07 1LETCO MEDICAL, LLC
08 1Medisca Inc.
09 2Professional Compounding Centers of America dba PCCA
10 1Spectrum Laboratory Products, Inc.
11 1Zhejiang Cheng Yi Pharmaceutical Co., Ltd
01 5AZATHIOPRINE
02 6Azathioprine
03 1azathioprine
01 2China
02 1Finland
03 2India
04 1Luxembourg
05 1South Africa
06 3U.S.A
07 2United Kingdom
NDC Package Code : 12780-0300
Start Marketing Date : 1997-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48954-909
Start Marketing Date : 1993-02-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-0732
Start Marketing Date : 2004-02-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-143
Start Marketing Date : 2010-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46014-1110
Start Marketing Date : 2009-11-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2189
Start Marketing Date : 2011-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0312
Start Marketing Date : 2014-08-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0071
Start Marketing Date : 2020-02-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2258
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-0783
Start Marketing Date : 1997-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Azathioprine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azathioprine, including repackagers and relabelers. The FDA regulates Azathioprine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azathioprine 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 Azathioprine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azathioprine supplier is an individual or a company that provides Azathioprine active pharmaceutical ingredient (API) or Azathioprine finished formulations upon request. The Azathioprine suppliers may include Azathioprine API manufacturers, exporters, distributors and traders.
click here to find a list of Azathioprine 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 Azathioprine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Azathioprine 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 Azathioprine 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 Azathioprine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Azathioprine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Azathioprine suppliers with NDC on PharmaCompass.
We have 11 companies offering Azathioprine
Get in contact with the supplier of your choice:
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