Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Eli Lilly
03 1FDC
04 1GLAND PHARMA LIMITED
05 1Helsinn Advanced Synthesis
06 1Jinan Jinda Pharmaceutical Chemistry Co Ltd
07 1ScinoPharm Taiwan Ltd
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 : 33845
Submission : 2019-06-17
Status :
Type : II
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PharmaCompass offers a list of Dantrolene 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 Dantrolene manufacturer or Dantrolene supplier for your needs.
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PharmaCompass also assists you with knowing the Dantrolene API Price utilized in the formulation of products. Dantrolene API Price is not always fixed or binding as the Dantrolene Price is obtained through a variety of data sources. The Dantrolene Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A REVONTO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of REVONTO, including repackagers and relabelers. The FDA regulates REVONTO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. REVONTO 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 REVONTO supplier is an individual or a company that provides REVONTO active pharmaceutical ingredient (API) or REVONTO finished formulations upon request. The REVONTO suppliers may include REVONTO API manufacturers, exporters, distributors and traders.
click here to find a list of REVONTO suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A REVONTO DMF (Drug Master File) is a document detailing the whole manufacturing process of REVONTO active pharmaceutical ingredient (API) in detail. Different forms of REVONTO DMFs exist exist since differing nations have different regulations, such as REVONTO USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A REVONTO DMF submitted to regulatory agencies in the US is known as a USDMF. REVONTO USDMF includes data on REVONTO's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The REVONTO USDMF is kept confidential to protect the manufacturer’s intellectual property.
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