Visitor Monitoring Drug Details: NEGGRAM
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: NEGGRAM
FDA Application No: (NDA) 014214
Active Ingredient(s): NALIDIXIC ACID
Company: SANOFI AVENTIS US
Original Approval or Tentative Approval Date: March 6, 1964
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority 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
NEGGRAM NALIDIXIC ACID250MGTABLET; ORAL Prescription No AB
NEGGRAM NALIDIXIC ACID500MGTABLET; ORAL Prescription No AB
NEGGRAM NALIDIXIC ACID1GMTABLET; ORAL Prescription Yes AB


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