Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences
02 1Aarti Pharmalabs
03 1Cambrex Corporation
04 1Chemi SpA
05 1Emcure Pharmaceuticals
06 1JUHUA GROUP CORP PHARMACEUTICAL FACTORY
07 1Merck & Co
08 1Viatris
09 1Zambon Group SpA
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34818
Submission : 2020-04-20
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24762
Submission : 2011-03-15
Status :
Type : II
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PharmaCompass offers a list of Diflunisal 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 Diflunisal manufacturer or Diflunisal supplier for your needs.
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PharmaCompass also assists you with knowing the Diflunisal API Price utilized in the formulation of products. Diflunisal API Price is not always fixed or binding as the Diflunisal Price is obtained through a variety of data sources. The Diflunisal Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A MK 647 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK 647, including repackagers and relabelers. The FDA regulates MK 647 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK 647 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 MK 647 supplier is an individual or a company that provides MK 647 active pharmaceutical ingredient (API) or MK 647 finished formulations upon request. The MK 647 suppliers may include MK 647 API manufacturers, exporters, distributors and traders.
click here to find a list of MK 647 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MK 647 DMF (Drug Master File) is a document detailing the whole manufacturing process of MK 647 active pharmaceutical ingredient (API) in detail. Different forms of MK 647 DMFs exist exist since differing nations have different regulations, such as MK 647 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MK 647 DMF submitted to regulatory agencies in the US is known as a USDMF. MK 647 USDMF includes data on MK 647's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MK 647 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MK 647 suppliers with USDMF on PharmaCompass.
We have 9 companies offering MK 647
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