Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International Inc
02 1Chinoin Pharmaceutical and Chemical Works Private Co., Ltd.
03 1EUROAPI Hungary Ltd.
04 1DARMERICA, LLC
05 1Everlight Chemical Industrial Corporation Kuanyin II Plant
06 1LETCO MEDICAL, LLC
07 1Medisca Inc.
08 1Ono Pharmaceutical Co., Ltd.
09 1Pharmacia and Upjohn Company LLC
10 1Professional Compounding Centers of America dba PCCA
11 1Qingdao Biopeptek Co., Ltd.
12 1Spectrum Laboratory Products, Inc.
13 1YS Life Science Co., Ltd.
01 2ALPROSTADIL
02 10Alprostadil
03 1Alprostadil Prostaglandin E1
01 2France
02 1Japan
03 1South Korea
04 2Taiwan
05 6U.S.A
06 1United Kingdom
Chirogate is a professional Prostaglandin manufacturer.
NDC Package Code : 68245-0007
Start Marketing Date : 2005-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 45542-1152
Start Marketing Date : 2014-10-28
End Marketing Date : 2025-09-20
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82231-101
Start Marketing Date : 2014-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1128
Start Marketing Date : 2009-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1mg/mg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0944
Start Marketing Date : 2017-08-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 63902-100
Start Marketing Date : 2012-01-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2196
Start Marketing Date : 2013-06-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 0009-0042
Start Marketing Date : 2015-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-0073
Start Marketing Date : 1997-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10mg/10mg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 40016-010
Start Marketing Date : 2016-05-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Alprostadil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alprostadil, including repackagers and relabelers. The FDA regulates Alprostadil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alprostadil 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 Alprostadil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Alprostadil supplier is an individual or a company that provides Alprostadil active pharmaceutical ingredient (API) or Alprostadil finished formulations upon request. The Alprostadil suppliers may include Alprostadil API manufacturers, exporters, distributors and traders.
click here to find a list of Alprostadil 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 Alprostadil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Alprostadil 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 Alprostadil 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 Alprostadil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Alprostadil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Alprostadil suppliers with NDC on PharmaCompass.
We have 12 companies offering Alprostadil
Get in contact with the supplier of your choice:
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