Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
01 1Cayman Pharma s r.o.
02 1EUROAPI Hungary Ltd.
03 1MSN Laboratories Private Limited
04 1Pharmacia and Upjohn Company LLC
05 1SUN PHARMACEUTICAL INDUSTRIES, INC.
06 1Sai Life Sciences Limited
07 1Wasserburger Arzneimittelwerk GmbH
01 1Epoprostenol
02 5Epoprostenol Sodium
03 1Epoprostenol sodium
01 1Czech Republic
02 1France
03 3India
04 1Sweden
05 1U.S.A
Cayman Pharma is Europe's most reliable and versatile source for Prostaglandin APIs//FDA approved.
NDC Package Code : 61556-030
Start Marketing Date : 2011-04-06
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 : 82231-106
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 : 54893-0004
Start Marketing Date : 2011-09-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0009-5164
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62287-123
Start Marketing Date : 2010-04-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (1.5mg/10mL)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 14474-025
Start Marketing Date : 2012-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62756-033
Start Marketing Date : 2021-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
59
PharmaCompass offers a list of Epoprostenol Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Epoprostenol Sodium manufacturer or Epoprostenol Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Epoprostenol Sodium manufacturer or Epoprostenol Sodium supplier.
PharmaCompass also assists you with knowing the Epoprostenol Sodium API Price utilized in the formulation of products. Epoprostenol Sodium API Price is not always fixed or binding as the Epoprostenol Sodium Price is obtained through a variety of data sources. The Epoprostenol Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Flolan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flolan, including repackagers and relabelers. The FDA regulates Flolan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flolan 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 Flolan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flolan supplier is an individual or a company that provides Flolan active pharmaceutical ingredient (API) or Flolan finished formulations upon request. The Flolan suppliers may include Flolan API manufacturers, exporters, distributors and traders.
click here to find a list of Flolan 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 Flolan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Flolan 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 Flolan 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 Flolan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flolan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Flolan suppliers with NDC on PharmaCompass.
We have 7 companies offering Flolan
Get in contact with the supplier of your choice:
