Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
01 1Trientine Tetrahydrochloride
01 1India
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-093
Start Marketing Date : 2022-10-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
A Trientine Tetrahydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trientine Tetrahydrochloride, including repackagers and relabelers. The FDA regulates Trientine Tetrahydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trientine Tetrahydrochloride supplier is an individual or a company that provides Trientine Tetrahydrochloride active pharmaceutical ingredient (API) or Trientine Tetrahydrochloride finished formulations upon request. The Trientine Tetrahydrochloride suppliers may include Trientine Tetrahydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride 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 Trientine Tetrahydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trientine Tetrahydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trientine Tetrahydrochloride suppliers with NDC on PharmaCompass.
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