01 1Interquim, S.A. de C.V.
02 1Suven Pharmaceuticals Limited
01 2Rifapentine
01 1India
02 1Mexico
NDC Package Code : 40074-0009
Start Marketing Date : 2021-09-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68022-7055
Start Marketing Date : 2016-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
13
PharmaCompass offers a list of Rifapentine 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 Rifapentine manufacturer or Rifapentine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rifapentine manufacturer or Rifapentine supplier.
PharmaCompass also assists you with knowing the Rifapentine API Price utilized in the formulation of products. Rifapentine API Price is not always fixed or binding as the Rifapentine Price is obtained through a variety of data sources. The Rifapentine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RPT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RPT, including repackagers and relabelers. The FDA regulates RPT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RPT 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 RPT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RPT supplier is an individual or a company that provides RPT active pharmaceutical ingredient (API) or RPT finished formulations upon request. The RPT suppliers may include RPT API manufacturers, exporters, distributors and traders.
click here to find a list of RPT 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 RPT as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for RPT 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 RPT 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 RPT and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a RPT NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of RPT suppliers with NDC on PharmaCompass.
We have 2 companies offering RPT
Get in contact with the supplier of your choice:
