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

Drug Name: NOVRAD
FDA Application No: (NDA) 012928
Active Ingredient(s): LEVOPROPOXYPHENE NAPSYLATE, ANHYDROUS
Company: LILLY
Original Approval or Tentative Approval Date: March 21, 1962
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Labels are not available
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
NOVRAD LEVOPROPOXYPHENE NAPSYLATE, ANHYDROUSEQ 50MG BASE/5MLSUSPENSION; ORAL Discontinued No None
NOVRAD LEVOPROPOXYPHENE NAPSYLATE, ANHYDROUSEQ 100MG BASECAPSULE; ORAL Discontinued No None
NOVRAD LEVOPROPOXYPHENE NAPSYLATE, ANHYDROUSEQ 50MG BASECAPSULE; ORAL Discontinued No None


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