Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania S.A.
02 1Veranova, L.P.
03 1Dr. Reddy's Laboratories Limited
04 1Pfanstiehl, Inc.
05 1Emcure Pharmaceuticals Limited
06 1Jiangsu Hansoh Pharmaceutical Group Co., Ltd.
07 1MSN Laboratories Private Limited
08 1SHILPA PHARMA LIFESCIENCES LIMITED
09 1SciAnda (Changshu) Pharmaceuticals, Ltd.
10 2ScinoPharm Taiwan Ltd.
11 1Sionc Pharmaceutical Private Limited
12 1Wuhan Biocause Pharmaceutical Development Co., Ltd
01 1DECITABINE
02 11Decitabine
03 1Decitabine Monohydrate
01 2China
02 5India
03 1Spain
04 3Taiwan
05 2U.S.A
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
NDC Package Code : 17404-1029
Start Marketing Date : 2022-07-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 50137-4147
Start Marketing Date : 2017-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-915
Start Marketing Date : 2010-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
NDC Package Code : 67430-275
Start Marketing Date : 2017-01-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-861
Start Marketing Date : 2023-12-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51916-360
Start Marketing Date : 2014-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0056
Start Marketing Date : 2017-01-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54245-7035
Start Marketing Date : 2013-06-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1223
Start Marketing Date : 2008-11-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1223
Start Marketing Date : 2008-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Decitabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Decitabine, including repackagers and relabelers. The FDA regulates Decitabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Decitabine 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 Decitabine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Decitabine supplier is an individual or a company that provides Decitabine active pharmaceutical ingredient (API) or Decitabine finished formulations upon request. The Decitabine suppliers may include Decitabine API manufacturers, exporters, distributors and traders.
click here to find a list of Decitabine 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 Decitabine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Decitabine 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 Decitabine 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 Decitabine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Decitabine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Decitabine suppliers with NDC on PharmaCompass.
We have 11 companies offering Decitabine
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