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 1Biophore India Pharmaceuticals Pvt Ltd
03 1Actavis Inc
04 1Apothecon Pharmaceuticals
05 1BrightGene Bio-Medical Technology Co.,Ltd
06 1Curia
07 1Dasami Lab
08 1Emcure Pharmaceuticals
09 1MSN Laboratories
10 1ORGANICA Feinchemie GmbH Wolfen
11 1Suven Life Sciences Limited
12 1Viatris
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Complete
Rev. Date : 2016-12-23
Pay. Date : 2016-09-13
DMF Number : 30878
Submission : 2016-11-08
Status :
Type : II
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Complete
Rev. Date : 2016-03-01
Pay. Date : 2015-09-15
DMF Number : 29527
Submission : 2015-09-03
Status :
Type : II
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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 Trientine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trientine, including repackagers and relabelers. The FDA regulates Trientine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trientine 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trientine supplier is an individual or a company that provides Trientine active pharmaceutical ingredient (API) or Trientine finished formulations upon request. The Trientine suppliers may include Trientine API manufacturers, exporters, distributors and traders.
click here to find a list of Trientine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Trientine DMF (Drug Master File) is a document detailing the whole manufacturing process of Trientine active pharmaceutical ingredient (API) in detail. Different forms of Trientine DMFs exist exist since differing nations have different regulations, such as Trientine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Trientine DMF submitted to regulatory agencies in the US is known as a USDMF. Trientine USDMF includes data on Trientine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Trientine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Trientine suppliers with USDMF on PharmaCompass.
We have 12 companies offering Trientine
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