Visitor Monitoring Drug Details: MACRODANTIN
 
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Drug Details

Drug Name: MACRODANTIN
FDA Application No: (NDA) 016620
Active Ingredient(s): NITROFURANTOIN, MACROCRYSTALLINE
Company: PROCTER AND GAMBLE
Original Approval or Tentative Approval Date: June 5, 1970
Chemical Type: 3 New dosage form
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
MACRODANTIN NITROFURANTOIN, MACROCRYSTALLINE50MGCAPSULE; ORAL Prescription No AB
MACRODANTIN NITROFURANTOIN, MACROCRYSTALLINE100MGCAPSULE; ORAL Prescription Yes AB
MACRODANTIN NITROFURANTOIN, MACROCRYSTALLINE25MGCAPSULE; ORAL Prescription No AB


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