Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International Inc
02 1NURAY CHEMICALS PRIVATE LIMITED
03 1Everlight Chemical Industrial Corporation Kuanyin II Plant
04 1MSN Laboratories Private Limited
05 1TIEN (Tianjin) Pharmaceutical Co. Ltd
01 2Treprostinil Diethanolamine
02 3Treprostinil Diolamine
01 1China
02 2India
03 2Taiwan
Chirogate is a professional Prostaglandin manufacturer.
NDC Package Code : 68245-0010
Start Marketing Date : 2010-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-036
Start Marketing Date : 2024-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65035-149
Start Marketing Date : 2016-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0029
Start Marketing Date : 2015-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69870-108
Start Marketing Date : 2018-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Treprostinil Diolamine 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 Treprostinil Diolamine manufacturer or Treprostinil Diolamine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Treprostinil Diolamine manufacturer or Treprostinil Diolamine supplier.
PharmaCompass also assists you with knowing the Treprostinil Diolamine API Price utilized in the formulation of products. Treprostinil Diolamine API Price is not always fixed or binding as the Treprostinil Diolamine Price is obtained through a variety of data sources. The Treprostinil Diolamine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Treprostinil Diolamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Treprostinil Diolamine, including repackagers and relabelers. The FDA regulates Treprostinil Diolamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Treprostinil Diolamine 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 Treprostinil Diolamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Treprostinil Diolamine supplier is an individual or a company that provides Treprostinil Diolamine active pharmaceutical ingredient (API) or Treprostinil Diolamine finished formulations upon request. The Treprostinil Diolamine suppliers may include Treprostinil Diolamine API manufacturers, exporters, distributors and traders.
click here to find a list of Treprostinil Diolamine 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 Treprostinil Diolamine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Treprostinil Diolamine 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 Treprostinil Diolamine 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 Treprostinil Diolamine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Treprostinil Diolamine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Treprostinil Diolamine suppliers with NDC on PharmaCompass.
We have 5 companies offering Treprostinil Diolamine
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