Visitor Monitoring Drug Details: BAYCOL
 
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Drug Details

Drug Name: BAYCOL
FDA Application No: (NDA) 020740
Active Ingredient(s): CERIVASTATIN SODIUM
Company: BAYER PHARMS
Original Approval or Tentative Approval Date: June 26, 1997
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
BAYCOL CERIVASTATIN SODIUM0.05MGTABLET; ORAL Discontinued No None
BAYCOL CERIVASTATIN SODIUM0.1MGTABLET; ORAL Discontinued No None
BAYCOL CERIVASTATIN SODIUM0.2MGTABLET; ORAL Discontinued No None
BAYCOL CERIVASTATIN SODIUM0.3MGTABLET; ORAL Discontinued No None
BAYCOL CERIVASTATIN SODIUM0.4MGTABLET; ORAL Discontinued No None
BAYCOL CERIVASTATIN SODIUM0.8MGTABLET; ORAL Discontinued No None


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