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

Drug Name: UCEPHAN
FDA Application No: (NDA) 019530
Active Ingredient(s): SODIUM BENZOATE; SODIUM PHENYLACETATE
Company: B BRAUN
Original Approval or Tentative Approval Date: December 23, 1987
Chemical Type: 14 New molecular entity and new combination
Review Classification: P Priority review drug
O Orphan 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
UCEPHAN SODIUM BENZOATE; SODIUM PHENYLACETATE100MG/ML; 100MG/MLSOLUTION; ORAL Discontinued No None


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