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

Drug Name: PROZAC
FDA Application No: (NDA) 020974
Active Ingredient(s): FLUOXETINE HYDROCHLORIDE
Company: LILLY
Original Approval or Tentative Approval Date: March 9, 1999
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
PROZAC FLUOXETINE HYDROCHLORIDEEQ 10MG BASETABLET; ORAL Discontinued No None
PROZAC FLUOXETINE HYDROCHLORIDEEQ 20MG BASE **Federal Register determination that product was not discontinued or withdraw for safety or efficacy reasons**TABLET; ORAL Discontinued No None


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