Visitor Monitoring Drug Details: PHENERGAN
 
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Drug Details

Drug Name: PHENERGAN
FDA Application No: (NDA) 010926
Active Ingredient(s): PROMETHAZINE HYDROCHLORIDE
Company: WYETH PHARMS INC
Original Approval or Tentative Approval Date: May 5, 1958
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no 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
PHENERGAN PROMETHAZINE HYDROCHLORIDE25MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**SUPPOSITORY; RECTAL Discontinued No None
PHENERGAN PROMETHAZINE HYDROCHLORIDE12.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**SUPPOSITORY; RECTAL Discontinued No None


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