TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1Teva API India Limited
02 1Aurobindo Pharma Limited
01 2Triheptanoin
01 1India
02 1Israel
TAPI offers customized CDMO Solutions for API development and manufacturing services.
NDC Package Code : 15894-0041
Start Marketing Date : 2024-01-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-938
Start Marketing Date : 2024-01-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
A Triheptanoin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triheptanoin, including repackagers and relabelers. The FDA regulates Triheptanoin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triheptanoin 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 Triheptanoin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triheptanoin supplier is an individual or a company that provides Triheptanoin active pharmaceutical ingredient (API) or Triheptanoin finished formulations upon request. The Triheptanoin suppliers may include Triheptanoin API manufacturers, exporters, distributors and traders.
click here to find a list of Triheptanoin 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 Triheptanoin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Triheptanoin 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 Triheptanoin 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 Triheptanoin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Triheptanoin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Triheptanoin suppliers with NDC on PharmaCompass.
We have 2 companies offering Triheptanoin
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