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PharmaCompass offers a list of Tetracaine 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 Tetracaine manufacturer or Tetracaine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetracaine manufacturer or Tetracaine supplier.
PharmaCompass also assists you with knowing the Tetracaine API Price utilized in the formulation of products. Tetracaine API Price is not always fixed or binding as the Tetracaine Price is obtained through a variety of data sources. The Tetracaine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 0619F35CGV manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0619F35CGV, including repackagers and relabelers. The FDA regulates 0619F35CGV manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0619F35CGV 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 0619F35CGV manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 0619F35CGV supplier is an individual or a company that provides 0619F35CGV active pharmaceutical ingredient (API) or 0619F35CGV finished formulations upon request. The 0619F35CGV suppliers may include 0619F35CGV API manufacturers, exporters, distributors and traders.
click here to find a list of 0619F35CGV 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 0619F35CGV as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 0619F35CGV 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 0619F35CGV 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 0619F35CGV and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 0619F35CGV NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 0619F35CGV suppliers with NDC on PharmaCompass.
We have 11 companies offering 0619F35CGV
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