Visitor Monitoring Drug Details: LANOXIN
 
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Drug Details

Drug Name: LANOXIN
FDA Application No: (NDA) 020405
Active Ingredient(s): DIGOXIN
Company: SMITHKLINE BEECHAM
Original Approval or Tentative Approval Date: September 30, 1997
Chemical Type: 7 Drug already marketed, but without an approved NDA
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
LANOXIN DIGOXIN0.0625MGTABLET; ORAL Discontinued No None
LANOXIN DIGOXIN0.125MGTABLET; ORAL Prescription No AB
LANOXIN DIGOXIN0.1875MGTABLET; ORAL Discontinued No None
LANOXIN DIGOXIN0.25MGTABLET; ORAL Prescription Yes AB
LANOXIN DIGOXIN0.375MGTABLET; ORAL Discontinued No None
LANOXIN DIGOXIN0.5MGTABLET; ORAL Discontinued No None


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