Visitor Monitoring Drug Details: AMOXIL
 
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Drug Details

Drug Name: AMOXIL
FDA Application No: (NDA) 050542
Active Ingredient(s): AMOXICILLIN
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: October 21, 1980
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
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
AMOXIL AMOXICILLIN250MGTABLET, CHEWABLE; ORAL Discontinued No None
AMOXIL AMOXICILLIN125MGTABLET, CHEWABLE; ORAL Discontinued No None


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