Visitor Monitoring Drug Details: BENADRYL
 
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Drug Details

Drug Name: BENADRYL
FDA Application No: (NDA) 005845
Active Ingredient(s): DIPHENHYDRAMINE HYDROCHLORIDE
Company: MCNEIL CONS
Original Approval or Tentative Approval Date: March 4, 1946
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
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
BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE50MGCAPSULE; ORAL Discontinued No None
BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE12.5MG/5MLELIXIR; ORAL Discontinued No None
BENADRYL DIPHENHYDRAMINE HYDROCHLORIDE25MGCAPSULE; ORAL Discontinued No None


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