Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Catalana SL
02 1Dipharma Francis Srl
03 1Ipca Laboratories Limited
01 1TRIAMTERENE
02 2Triamterene
01 1India
02 1Italy
03 1Spain
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0703
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0034
Start Marketing Date : 1980-01-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1197
Start Marketing Date : 2011-05-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Triamterene manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triamterene, including repackagers and relabelers. The FDA regulates Triamterene manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triamterene 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 Triamterene manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triamterene supplier is an individual or a company that provides Triamterene active pharmaceutical ingredient (API) or Triamterene finished formulations upon request. The Triamterene suppliers may include Triamterene API manufacturers, exporters, distributors and traders.
click here to find a list of Triamterene 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 Triamterene as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Triamterene 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 Triamterene 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 Triamterene and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Triamterene NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Triamterene suppliers with NDC on PharmaCompass.
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