01 1ACIC Europe API & Pharmaceuticals
02 1Industriale Chimica
03 1Medimpex
04 1ORGAMOL PHARMA SOLUTIONS SA
05 1Blank
01 1CHLOFIBRATE USP
02 2CLOFIBRATE
03 1CLOFIBRATE B/P/USP/NF
04 1CLOFIBRATE USP
01 1Cyprus
02 1Italy
03 1Switzerland
04 1United Kingdom
05 1Blank
01 5Inactive
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2976
Submission : 1977-06-23
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5407
Submission : 1984-04-20
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2710
Submission : 1976-07-19
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5852
Submission : 1985-05-22
Status : Inactive
Type : II
USDMF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5165
Submission : 1983-11-10
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
44
PharmaCompass offers a list of Clofibrate 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 Clofibrate manufacturer or Clofibrate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Clofibrate manufacturer or Clofibrate supplier.
PharmaCompass also assists you with knowing the Clofibrate API Price utilized in the formulation of products. Clofibrate API Price is not always fixed or binding as the Clofibrate Price is obtained through a variety of data sources. The Clofibrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Negalip manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Negalip, including repackagers and relabelers. The FDA regulates Negalip manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Negalip API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Negalip supplier is an individual or a company that provides Negalip active pharmaceutical ingredient (API) or Negalip finished formulations upon request. The Negalip suppliers may include Negalip API manufacturers, exporters, distributors and traders.
click here to find a list of Negalip suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Negalip DMF (Drug Master File) is a document detailing the whole manufacturing process of Negalip active pharmaceutical ingredient (API) in detail. Different forms of Negalip DMFs exist exist since differing nations have different regulations, such as Negalip USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Negalip DMF submitted to regulatory agencies in the US is known as a USDMF. Negalip USDMF includes data on Negalip's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Negalip USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Negalip suppliers with USDMF on PharmaCompass.
We have 4 companies offering Negalip
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