Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Bioindustria L.I.M. Spa
03 1Dishman Carbogen Amcis
04 1Industriale Chimica
05 1Ipca Laboratories
06 1Quimica Sintetica
07 1Servier
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38609
Submission : 2023-07-31
Status :
Type : II
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PharmaCompass offers a list of Indapamide 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 Indapamide manufacturer or Indapamide supplier for your needs.
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PharmaCompass also assists you with knowing the Indapamide API Price utilized in the formulation of products. Indapamide API Price is not always fixed or binding as the Indapamide Price is obtained through a variety of data sources. The Indapamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tertensif manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tertensif, including repackagers and relabelers. The FDA regulates Tertensif manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tertensif API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tertensif supplier is an individual or a company that provides Tertensif active pharmaceutical ingredient (API) or Tertensif finished formulations upon request. The Tertensif suppliers may include Tertensif API manufacturers, exporters, distributors and traders.
click here to find a list of Tertensif suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tertensif DMF (Drug Master File) is a document detailing the whole manufacturing process of Tertensif active pharmaceutical ingredient (API) in detail. Different forms of Tertensif DMFs exist exist since differing nations have different regulations, such as Tertensif USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Tertensif DMF submitted to regulatory agencies in the US is known as a USDMF. Tertensif USDMF includes data on Tertensif's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Tertensif USDMF is kept confidential to protect the manufacturer’s intellectual property.
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