01 1MSN Life Sciences Private Limited
01 1Tafenoquine Succinate
01 1India
NDC Package Code : 69766-079
Start Marketing Date : 2020-09-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Tafenoquine Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tafenoquine Succinate, including repackagers and relabelers. The FDA regulates Tafenoquine Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tafenoquine Succinate 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 Tafenoquine Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tafenoquine Succinate supplier is an individual or a company that provides Tafenoquine Succinate active pharmaceutical ingredient (API) or Tafenoquine Succinate finished formulations upon request. The Tafenoquine Succinate suppliers may include Tafenoquine Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Tafenoquine Succinate 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 Tafenoquine Succinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tafenoquine Succinate 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 Tafenoquine Succinate 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 Tafenoquine Succinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tafenoquine Succinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tafenoquine Succinate suppliers with NDC on PharmaCompass.
We have 1 companies offering Tafenoquine Succinate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
