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
 
Therapeutic Equivalents Label Information
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
TAGAMET HB CIMETIDINE100MGTABLET; ORAL Discontinued No None
TAGAMET HB CIMETIDINE200MGTABLET; ORAL OTC Yes None


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