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 1Apothecon Pharmaceuticals Pvt Ltd
03 1Azico Biophore India Private Limited
04 1Curia New York, Inc.
05 1Dasami Lab Private Limited
06 1Emcure Pharmaceuticals Limited
07 2MSN Organics Private Limited
08 1Optimus Drugs Private Limited
09 1Suven Pharmaceuticals Limited
01 2TRIENTINE HYDROCHLORIDE
02 7Trientine Hydrochloride
03 1Trientine Tetrahydrochloride
01 9India
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 : 76339-133
Start Marketing Date : 2019-09-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (9.999kg/9.999kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4003
Start Marketing Date : 2015-11-25
End Marketing Date : 2025-12-31
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 : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0017
Start Marketing Date : 2015-10-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0025
Start Marketing Date : 2023-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-026
Start Marketing Date : 2019-12-26
End Marketing Date : 2025-12-31
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...
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PharmaCompass offers a list of Trientine Hydrochloride 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 Trientine Hydrochloride manufacturer or Trientine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trientine Hydrochloride manufacturer or Trientine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Trientine Hydrochloride API Price utilized in the formulation of products. Trientine Hydrochloride API Price is not always fixed or binding as the Trientine Hydrochloride Price is obtained through a variety of data sources. The Trientine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MK-681 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK-681, including repackagers and relabelers. The FDA regulates MK-681 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK-681 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 MK-681 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MK-681 supplier is an individual or a company that provides MK-681 active pharmaceutical ingredient (API) or MK-681 finished formulations upon request. The MK-681 suppliers may include MK-681 API manufacturers, exporters, distributors and traders.
click here to find a list of MK-681 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 MK-681 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for MK-681 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 MK-681 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 MK-681 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a MK-681 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of MK-681 suppliers with NDC on PharmaCompass.
We have 9 companies offering MK-681
Get in contact with the supplier of your choice:
