Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
01 1Farmhispania, S.A.
02 1Curia New York, Inc.
03 1Huzhou Zhanwang Pharmaceutical Co., Ltd.
04 1W. R. Grace & Co.-Conn.
05 1Wuhan Biocause Pharmaceutical Development Co., Ltd
01 5Milrinone
01 2China
02 1Spain
03 2U.S.A
NDC Package Code : 17404-0017
Start Marketing Date : 2004-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65392-2202
Start Marketing Date : 1986-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1127
Start Marketing Date : 2006-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51916-312
Start Marketing Date : 2007-07-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63660-0002
Start Marketing Date : 2011-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Milrinone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Milrinone, including repackagers and relabelers. The FDA regulates Milrinone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Milrinone 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 Milrinone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Milrinone supplier is an individual or a company that provides Milrinone active pharmaceutical ingredient (API) or Milrinone finished formulations upon request. The Milrinone suppliers may include Milrinone API manufacturers, exporters, distributors and traders.
click here to find a list of Milrinone 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 Milrinone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Milrinone 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 Milrinone 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 Milrinone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Milrinone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Milrinone suppliers with NDC on PharmaCompass.
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