Visitor Monitoring Drug Details: PHENERGAN
 
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Drug Details

Drug Name: PHENERGAN
FDA Application No: (NDA) 007935
Active Ingredient(s): PROMETHAZINE HYDROCHLORIDE
Company: WYETH PHARMS INC
Original Approval or Tentative Approval Date: March 29, 1951
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
PHENERGAN PROMETHAZINE HYDROCHLORIDE12.5MGTABLET; ORAL Discontinued No None
PHENERGAN PROMETHAZINE HYDROCHLORIDE25MGTABLET; ORAL Prescription No AB
PHENERGAN PROMETHAZINE HYDROCHLORIDE50MGTABLET; ORAL Discontinued No None


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