Visitor Monitoring Drug Details: GLUCOPHAGE
 
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Drug Details

Drug Name: GLUCOPHAGE
FDA Application No: (NDA) 020357
Active Ingredient(s): METFORMIN HYDROCHLORIDE
Company: BRISTOL MYERS SQUIBB
Original Approval or Tentative Approval Date: March 3, 1995
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
GLUCOPHAGE METFORMIN HYDROCHLORIDE500MGTABLET; ORAL Prescription No AB
GLUCOPHAGE METFORMIN HYDROCHLORIDE850MGTABLET; ORAL Prescription No AB
GLUCOPHAGE METFORMIN HYDROCHLORIDE625MGTABLET; ORAL Discontinued No None
GLUCOPHAGE METFORMIN HYDROCHLORIDE750MGTABLET; ORAL Discontinued No None
GLUCOPHAGE METFORMIN HYDROCHLORIDE1GMTABLET; ORAL Prescription Yes AB


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