Visitor Monitoring Drug Details: PHENERGAN
 
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Drug Details

Drug Name: PHENERGAN
FDA Application No: (NDA) 008857
Active Ingredient(s): PROMETHAZINE HYDROCHLORIDE
Company: WYETH AYERST
Original Approval or Tentative Approval Date: August 20, 1956
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
PHENERGAN PROMETHAZINE HYDROCHLORIDE25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None
PHENERGAN PROMETHAZINE HYDROCHLORIDE50MG/ML ***Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None


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