01 1CARDIOME DEVELOPMENT AG
01 1Switzerland
01 1Inactive
01 1Blank
01 1Blank
01 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19171
Submission : 2006-03-14
Status : Inactive
Type : II
A Vernakalant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vernakalant, including repackagers and relabelers. The FDA regulates Vernakalant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vernakalant 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 Vernakalant supplier is an individual or a company that provides Vernakalant active pharmaceutical ingredient (API) or Vernakalant finished formulations upon request. The Vernakalant suppliers may include Vernakalant API manufacturers, exporters, distributors and traders.
click here to find a list of Vernakalant suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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