01 1Eriochem S.A.
01 1VINDOLINE AND CATHARANTHINE MIXTURE (VYC)
01 1Argentina
01 1Inactive
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17407
Submission : 2004-05-27
Status : Inactive
Type : II
A Vindoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vindoline, including repackagers and relabelers. The FDA regulates Vindoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vindoline 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 Vindoline supplier is an individual or a company that provides Vindoline active pharmaceutical ingredient (API) or Vindoline finished formulations upon request. The Vindoline suppliers may include Vindoline API manufacturers, exporters, distributors and traders.
click here to find a list of Vindoline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Vindoline DMF (Drug Master File) is a document detailing the whole manufacturing process of Vindoline active pharmaceutical ingredient (API) in detail. Different forms of Vindoline DMFs exist exist since differing nations have different regulations, such as Vindoline USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vindoline DMF submitted to regulatory agencies in the US is known as a USDMF. Vindoline USDMF includes data on Vindoline's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vindoline USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Vindoline suppliers with USDMF on PharmaCompass.
We have 1 companies offering Vindoline
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?