01 1Industriale Chimica s.r.l.
02 1Zhejiang Ausun Pharmaceutical Co., Ltd.
01 2Tafluprost
01 1China
02 1Italy
NDC Package Code : 63190-0590
Start Marketing Date : 2012-02-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76397-013
Start Marketing Date : 2020-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Tafluprost 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 Tafluprost manufacturer or Tafluprost supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tafluprost manufacturer or Tafluprost supplier.
PharmaCompass also assists you with knowing the Tafluprost API Price utilized in the formulation of products. Tafluprost API Price is not always fixed or binding as the Tafluprost Price is obtained through a variety of data sources. The Tafluprost Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zioptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zioptan, including repackagers and relabelers. The FDA regulates Zioptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zioptan 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 Zioptan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zioptan supplier is an individual or a company that provides Zioptan active pharmaceutical ingredient (API) or Zioptan finished formulations upon request. The Zioptan suppliers may include Zioptan API manufacturers, exporters, distributors and traders.
click here to find a list of Zioptan 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 Zioptan as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zioptan 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 Zioptan 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 Zioptan and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zioptan NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zioptan suppliers with NDC on PharmaCompass.
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