Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International Inc
01 1Hexadecyl Treprostinil
01 1Taiwan
Chirogate is a professional Prostaglandin manufacturer.
NDC Package Code : 68245-0014
Start Marketing Date : 2014-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Treprostinil Palmitil API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Treprostinil Palmitil manufacturer or Treprostinil Palmitil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Treprostinil Palmitil manufacturer or Treprostinil Palmitil supplier.
A Treprostinil Palmitil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Treprostinil Palmitil, including repackagers and relabelers. The FDA regulates Treprostinil Palmitil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Treprostinil Palmitil API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Treprostinil Palmitil supplier is an individual or a company that provides Treprostinil Palmitil active pharmaceutical ingredient (API) or Treprostinil Palmitil finished formulations upon request. The Treprostinil Palmitil suppliers may include Treprostinil Palmitil API manufacturers, exporters, distributors and traders.
click here to find a list of Treprostinil Palmitil suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Palmitil as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Treprostinil Palmitil 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 Palmitil 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 Palmitil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Treprostinil Palmitil NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Treprostinil Palmitil suppliers with NDC on PharmaCompass.
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