Visitor Monitoring Drug Details: GLUMETZA
 
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Drug Details

Drug Name: GLUMETZA
FDA Application No: (NDA) 021748
Active Ingredient(s): METFORMIN HYDROCHLORIDE
Company: DEPOMED INC
Original Approval or Tentative Approval Date: June 3, 2005
Chemical Type: 5 New manufacturer
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
GLUMETZA METFORMIN HYDROCHLORIDE500MGTABLET, EXTENDED RELEASE; ORAL Prescription No BX
GLUMETZA METFORMIN HYDROCHLORIDE1GMTABLET, EXTENDED RELEASE; ORAL Prescription Yes BX


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