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
02 1APICORE PHARMACEUTICALS PRIVATE LIMITED
03 1Apothecon Pharmaceuticals Pvt Ltd
04 1Azico Biophore India Private Limited
05 1Curia New York, Inc.
06 1Dasami Lab Private Limited
07 1Emcure Pharmaceuticals Limited
08 2MSN Organics Private Limited
09 1Optimus Drugs Private Limited
10 1Suven Pharmaceuticals Limited
01 3TRIENTINE HYDROCHLORIDE
02 7Trientine Hydrochloride
03 1Trientine Tetrahydrochloride
01 10India
02 1U.S.A
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-031
Start Marketing Date : 2024-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-184
Start Marketing Date : 2017-07-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4003
Start Marketing Date : 2015-11-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65392-2901
Start Marketing Date : 1985-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70966-0016
Start Marketing Date : 1985-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-914
Start Marketing Date : 2023-09-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0017
Start Marketing Date : 2015-10-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0025
Start Marketing Date : 2023-03-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-026
Start Marketing Date : 2019-12-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68022-7052
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...
A Trientine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trientine Hydrochloride, including repackagers and relabelers. The FDA regulates Trientine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trientine Hydrochloride 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 Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trientine Hydrochloride supplier is an individual or a company that provides Trientine Hydrochloride active pharmaceutical ingredient (API) or Trientine Hydrochloride finished formulations upon request. The Trientine Hydrochloride suppliers may include Trientine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trientine Hydrochloride 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 Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trientine Hydrochloride 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 Hydrochloride 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 Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trientine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trientine Hydrochloride suppliers with NDC on PharmaCompass.
We have 10 companies offering Trientine Hydrochloride
Get in contact with the supplier of your choice:
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