Visitor Monitoring Drug Details: PROMETHEGAN
 
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Drug Details

Drug Name: PROMETHEGAN
FDA Application No: (ANDA) 087165
Active Ingredient(s): PROMETHAZINE HYDROCHLORIDE
Company: G AND W LABS
Original Approval or Tentative Approval Date: August 14, 1987
 
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
PROMETHEGAN PROMETHAZINE HYDROCHLORIDE50MGSUPPOSITORY; RECTAL Prescription Yes None


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