Visitor Monitoring Drug Details: TAGAMET HB
 
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Drug Details

Drug Name: TAGAMET HB
FDA Application No: (NDA) 020238
Active Ingredient(s): CIMETIDINE
Company: GLAXOSMITHKLINE
Original Approval or Tentative Approval Date: June 19, 1995
Chemical Type: 8 OTC (over-the-counter) switch
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
TAGAMET HB CIMETIDINE100MGTABLET; ORAL Discontinued No None
TAGAMET HB CIMETIDINE200MGTABLET; ORAL OTC Yes None


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